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dbVar

Database of genomic structural variation

nsv5982270

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:80

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: 131 SVs from 21 studies. See in: genome view

Submitted genomic202,867,909-202,867,988

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5982270	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	202,867,909	202,867,988
nsv5982270	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	202,837,037	202,837,116

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17521675	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17521675	Submitted genomic		NC_000001.11:g.202 867909_202867988de l	GRCh38 (hg38)		NC_000001.11	Chr1	202,867,909	202,867,988
nssv17521675	Remapped	Perfect	NC_000001.10:g.202 837037_202837116de l	GRCh37.p13	First Pass	NC_000001.10	Chr1	202,837,037	202,837,116

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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