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dbVar

Database of genomic structural variation

nsv6011327

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:293

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

Submitted genomic140,340,025-140,340,317

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6011327	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	140,340,025	140,340,317
nsv6011327	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	139,719,610	139,719,902

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17550316	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17550316	Submitted genomic		NC_000005.10:g.140 340025_140340317de l	GRCh38 (hg38)		NC_000005.10	Chr5	140,340,025	140,340,317
nssv17550316	Remapped	Perfect	NC_000005.9:g.1397 19610_139719902del	GRCh37.p13	First Pass	NC_000005.9	Chr5	139,719,610	139,719,902

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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