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dbVar

Database of genomic structural variation

nsv6005591

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:179,769

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: 498 SVs from 61 studies. See in: genome view

Submitted genomic90,353,849-90,533,617

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6005591	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	90,353,849	90,533,617
nsv6005591	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	92,113,606	92,293,374

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17585329	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17585329	Submitted genomic		NC_000010.11:g.903 53849_90533617dup	GRCh38 (hg38)		NC_000010.11	Chr10	90,353,849	90,533,617
nssv17585329	Remapped	Perfect	NC_000010.10:g.921 13606_92293374dup	GRCh37.p13	First Pass	NC_000010.10	Chr10	92,113,606	92,293,374

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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