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dbVar

Database of genomic structural variation

nsv6038011

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:7,153

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: 168 SVs from 39 studies. See in: genome view

Submitted genomic31,639,019-31,646,171

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6038011	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	31,639,019	31,646,171
nsv6038011	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	31,791,953	31,799,105

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17614324	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17614324	Submitted genomic		NC_000012.12:g.316 39019_31646171dup	GRCh38 (hg38)		NC_000012.12	Chr12	31,639,019	31,646,171
nssv17614324	Remapped	Perfect	NC_000012.11:g.317 91953_31799105dup	GRCh37.p13	First Pass	NC_000012.11	Chr12	31,791,953	31,799,105

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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