nsv4372116

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:50
Validation:Not tested
Clinical Assertions: No
Region Size:25,178

Publication(s):Zarrei et al. 2019

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 75 studies. See in: genome view

Remapped(Score: Perfect):19,934,473-19,959,650

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4372116	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nsv4372116	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	19,945,795	19,970,972

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15616099	copy number loss	1-0782-004	SNP array	Genotyping	15
nssv15617669	copy number loss	1-0836-003	SNP array	Genotyping	23
nssv15618354	copy number loss	1-0866-003	SNP array	Genotyping	14
nssv15620833	copy number loss	1-0959-003	SNP array	Genotyping	27
nssv15621604	copy number loss	1-1005-005	SNP array	Genotyping	22
nssv15627686	copy number loss	1-0533-003	SNP array	Genotyping	17
nssv15627720	copy number loss	1-0534-002	SNP array	Genotyping	23
nssv15631796	copy number loss	10-0015-003	SNP array	Genotyping	20
nssv15633998	copy number loss	11-0021-001	SNP array	Genotyping	27
nssv15634606	copy number loss	12-4310-001	SNP array	Genotyping	20
nssv15634896	copy number loss	12-4404-004	SNP array	Genotyping	25
nssv15636336	copy number loss	14-0039-004	SNP array	Genotyping	24
nssv15643652	copy number loss	2-0018-003	SNP array	Genotyping	23
nssv15644217	copy number loss	16-1004-001	SNP array	Genotyping	23
nssv15646501	copy number loss	2-1189-003	SNP array	Genotyping	24
nssv15646724	copy number loss	2-0305-004	SNP array	Genotyping	20
nssv15647988	copy number loss	2-1322-003	SNP array	Genotyping	23
nssv15648489	copy number loss	2-1330-002	SNP array	Genotyping	17
nssv15648528	copy number loss	2-1335-001	SNP array	Genotyping	23
nssv15649743	copy number loss	2-1334-002	SNP array	Genotyping	19
nssv15650243	copy number loss	2-1335-004	SNP array	Genotyping	33
nssv15651506	copy number loss	2-1437-004	SNP array	Genotyping	28
nssv15654038	copy number loss	2-1689-003	SNP array	Genotyping	23
nssv15654850	copy number loss	3-0522-000	SNP array	Genotyping	14
nssv15655364	copy number loss	3-0084-000	SNP array	Genotyping	25
nssv15656058	copy number loss	3-0607-000	SNP array	Genotyping	26
nssv15656783	copy number loss	3-0600-001	SNP array	Genotyping	22
nssv15657594	copy number loss	4-0039-001	SNP array	Genotyping	25
nssv15659587	copy number loss	3-0775-000	SNP array	Genotyping	18
nssv15665103	copy number loss	14AG81	SNP array	Genotyping	16
nssv15667095	copy number loss	7-0118-003	SNP array	Genotyping	21
nssv15667939	copy number loss	7-0160-003	SNP array	Genotyping	19
nssv15671542	copy number loss	7-0310-003	SNP array	Genotyping	14
nssv15673738	copy number loss	227576	SNP array	Genotyping	15
nssv15676783	copy number loss	174811	SNP array	Genotyping	18
nssv15677043	copy number loss	218117	SNP array	Genotyping	20
nssv15677059	copy number loss	218110	SNP array	Genotyping	20
nssv15677877	copy number loss	218116	SNP array	Genotyping	24
nssv15679127	copy number loss	182135	SNP array	Genotyping	19
nssv15679811	copy number loss	208585	SNP array	Genotyping	15
nssv15680594	copy number loss	215105	SNP array	Genotyping	32
nssv15681984	copy number loss	211605	SNP array	Genotyping	17
nssv15685166	copy number loss	OCD166-8961171	SNP array	Genotyping	18
nssv15687513	copy number loss	OCD162-896233	SNP array	Genotyping	13
nssv15688271	copy number loss	211604	SNP array	Genotyping	13
nssv15689409	copy number loss	OCD1004-S_896893	SNP array	Genotyping	18
nssv15692224	copy number loss	OCD67-896282	SNP array	Genotyping	14
nssv15699684	copy number loss	224898	SNP array	Genotyping	24
nssv15701523	copy number loss	150519	SNP array	Genotyping	15
nssv15702055	copy number loss	203861	SNP array	Genotyping	21

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15616099	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15617669	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15618354	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15620833	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15621604	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15627686	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15627720	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15631796	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15633998	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15634606	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15634896	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15636336	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15643652	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15644217	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15646501	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15646724	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15647988	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15648489	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15648528	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15649743	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15650243	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15651506	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15654038	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15654850	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15655364	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15656058	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15656783	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15657594	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15659587	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15665103	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15667095	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15667939	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15671542	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15673738	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15676783	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15677043	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15677059	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15677877	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15679127	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15679811	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15680594	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15681984	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15685166	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15687513	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15688271	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15689409	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15692224	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15699684	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15701523	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15702055	Remapped	Perfect	NC_000016.10:g.(?_ 19934473)_(1995965 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	19,934,473	19,959,650
nssv15616099	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15617669	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15618354	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15620833	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15621604	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15627686	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15627720	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15631796	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15633998	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15634606	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15634896	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15636336	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15643652	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15644217	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15646501	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15646724	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15647988	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15648489	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15648528	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15649743	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15650243	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15651506	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15654038	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15654850	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15655364	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15656058	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15656783	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15657594	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15659587	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15665103	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15667095	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15667939	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15671542	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15673738	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15676783	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15677043	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15677059	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15677877	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15679127	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15679811	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15680594	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15681984	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15685166	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15687513	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15688271	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15689409	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15692224	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15699684	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15701523	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972
nssv15702055	Submitted genomic		NC_000016.9:g.(?_1 9945795)_(19970972 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	19,945,795	19,970,972

dbVar

Database of genomic structural variation

nsv4372116

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

No genotype data were submitted for this variant