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dbVar

Database of genomic structural variation

nsv6012901

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:216,881

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: 1141 SVs from 82 studies. See in: genome view

Submitted genomic16,502,436-16,719,316

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6012901	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	16,502,436	16,719,316
nsv6012901	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	16,359,945	16,576,825

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17563690	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17563690	Submitted genomic		NC_000008.11:g.165 02436_16719316del	GRCh38 (hg38)		NC_000008.11	Chr8	16,502,436	16,719,316
nssv17563690	Remapped	Perfect	NC_000008.10:g.163 59945_16576825del	GRCh37.p13	First Pass	NC_000008.10	Chr8	16,359,945	16,576,825

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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