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dbVar

Database of genomic structural variation

nsv4703839

Organism: Homo sapiens

Study:nstd195 (Mwapagha et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:460,651

Publication(s):Mwapagha et al. 2021

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: 1224 SVs from 73 studies. See in: genome view

Remapped(Score: Perfect):37,466,333-37,926,983

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4703839	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	37,466,333	37,926,983
nsv4703839	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	37,323,851	37,784,501

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Copy number	Other Calls in this Sample and Study
nssv16242315	copy number variation	M478	Sequencing	Paired-end mapping	3	4,557

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16242315	Remapped	Perfect	GRCh38.p12	First Pass	NC_000008.11	Chr8	37,466,333	37,926,983
nssv16242315	Submitted genomic		GRCh37 (hg19)		NC_000008.10	Chr8	37,323,851	37,784,501

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.

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