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dbVar

Database of genomic structural variation

nsv5983932

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:117

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: 99 SVs from 23 studies. See in: genome view

Submitted genomic32,017,387-32,017,503

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5983932	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	32,017,387	32,017,503
nsv5983932	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	32,482,988	32,483,104

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17535949	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17535949	Submitted genomic		NC_000001.11:g.320 17387_32017503del	GRCh38 (hg38)		NC_000001.11	Chr1	32,017,387	32,017,503
nssv17535949	Remapped	Perfect	NC_000001.10:g.324 82988_32483104del	GRCh37.p13	First Pass	NC_000001.10	Chr1	32,482,988	32,483,104

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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