esv3877198

Organism: Homo sapiens

Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:52
Validation:Not tested
Clinical Assertions: No
Region Size:21,029

Publication(s):1000 Genomes Consortium Phase 3 Integrated SV

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 389 SVs from 54 studies. See in: genome view

Remapped(Score: Perfect):29,545,457-29,567,485

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3877198	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
esv3877198	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv23960846	deletion	HG01083	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,348
essv23960847	deletion	HG01111	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,414
essv23960848	deletion	HG01204	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,677
essv23960849	deletion	HG01269	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,343
essv23960850	deletion	HG01323	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,272
essv23960851	deletion	HG01375	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,366
essv23960852	deletion	HG01438	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,233
essv23960853	deletion	HG01459	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,404
essv23960854	deletion	HG01618	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,073
essv23960855	deletion	HG01886	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,702
essv23960856	deletion	HG01896	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,801
essv23960857	deletion	HG01921	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,224
essv23960858	deletion	HG01923	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,463
essv23960859	deletion	HG01926	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,396
essv23960860	deletion	HG01933	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,343
essv23960861	deletion	HG01961	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,329
essv23960862	deletion	HG01965	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,114
essv23960863	deletion	HG01968	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,970
essv23960864	deletion	HG01970	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,082
essv23960865	deletion	HG01977	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,218
essv23960866	deletion	HG01997	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,083
essv23960867	deletion	HG02002	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,315
essv23960868	deletion	HG02006	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,756
essv23960869	deletion	HG02008	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,539
essv23960870	deletion	HG02090	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,448
essv23960871	deletion	HG02102	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,446
essv23960872	deletion	HG02104	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,150
essv23960873	deletion	HG02147	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,149
essv23960874	deletion	HG02252	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,179
essv23960875	deletion	HG02260	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,293
essv23960876	deletion	HG02275	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,073
essv23960877	deletion	HG02285	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,401
essv23960878	deletion	HG02309	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,730
essv23960879	deletion	HG02323	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,049
essv23960880	deletion	HG02345	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,758
essv23960881	deletion	HG02568	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,026
essv23960882	deletion	HG02768	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,980
essv23960883	deletion	HG03455	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,774
essv23960884	deletion	NA19025	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,206
essv23960885	deletion	NA19038	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,670
essv23960886	deletion	NA19043	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,123
essv23960887	deletion	NA19189	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,039
essv23960888	deletion	NA19214	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,493
essv23960889	deletion	NA19222	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,939
essv23960890	deletion	NA19332	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,777
essv23960891	deletion	NA19463	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,890
essv23960892	deletion	NA19682	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,552
essv23960893	deletion	NA19740	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,228
essv23960894	deletion	NA19741	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,283
essv23960895	deletion	NA19777	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,562
essv23960896	deletion	NA19982	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,130
essv23960897	deletion	NA20294	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,120

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv23960846	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960847	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960848	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960849	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960850	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960851	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960852	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960853	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960854	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960855	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960856	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960857	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960858	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960859	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960860	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960861	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960862	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960863	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960864	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960865	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960866	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960867	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960868	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960869	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960870	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960871	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960872	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960873	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960874	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960875	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960876	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960877	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960878	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960879	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960880	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960881	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960882	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960883	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960884	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960885	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960886	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960887	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960888	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960889	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960890	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960891	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960892	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960893	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960894	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960895	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960896	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960897	Remapped	Perfect	NC_000016.10:g.(29 545457_29545957)_( 29566985_29567485) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,545,957 (-500, +0)	29,566,985 (-0, +500)
essv23960846	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960847	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960848	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960849	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960850	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960851	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960852	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960853	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960854	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960855	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960856	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960857	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960858	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960859	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960860	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960861	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960862	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960863	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960864	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960865	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960866	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960867	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960868	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960869	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960870	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960871	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960872	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960873	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960874	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960875	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960876	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960877	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960878	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960879	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960880	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960881	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960882	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960883	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960884	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960885	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960886	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960887	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960888	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960889	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960890	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960891	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960892	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)
essv23960893	Submitted genomic		NC_000016.9:g.(295 56778_29557278)_(2 9578306_29578806)d el	GRCh37 (hg19)		NC_000016.9	Chr16	29,557,278 (-500, +0)	29,578,306 (-0, +500)

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dbVar

Database of genomic structural variation

esv3877198

Links to Other Resources

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.