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dbVar

Database of genomic structural variation

nsv5995772

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:341

Publication(s):Wu 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: 187 SVs from 45 studies. See in: genome view

Submitted genomic163,155,889-163,156,229

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5995772	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	163,155,889	163,156,229
nsv5995772	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	164,077,041	164,077,381

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17541648	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17541648	Submitted genomic		NC_000004.12:g.163 155889_163156229de l	GRCh38 (hg38)		NC_000004.12	Chr4	163,155,889	163,156,229
nssv17541648	Remapped	Perfect	NC_000004.11:g.164 077041_164077381de l	GRCh37.p13	First Pass	NC_000004.11	Chr4	164,077,041	164,077,381

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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