Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6133211

Organism: Homo sapiens

Study:nstd213 (Pham et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,740,002

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: 4381 SVs from 102 studies. See in: genome view

Remapped(Score: Perfect):79,076,103-80,816,104

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6133211	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	79,076,103	80,816,104
nsv6133211	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	79,110,000	80,850,001

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17682901	copy number loss	SAMN20524657	Sequencing	Paired-end mapping	656

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17682901	Remapped	Perfect	NC_000016.10:g.790 76103_80816104del	GRCh38.p12	First Pass	NC_000016.10	Chr16	79,076,103	80,816,104
nssv17682901	Submitted genomic		NC_000016.9:g.7911 0000_80850001del	GRCh37 (hg19)		NC_000016.9	Chr16	79,110,000	80,850,001

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

You are here: NCBI