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dbVar

Database of genomic structural variation

nsv6019166

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:91,581

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: 307 SVs from 64 studies. See in: genome view

Submitted genomic26,937,239-27,028,819

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6019166	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	26,937,239	27,028,819
nsv6019166	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	26,905,018	26,996,598

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17575105	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17575105	Submitted genomic		NC_000006.12:g.269 37239_27028819dup	GRCh38 (hg38)		NC_000006.12	Chr6	26,937,239	27,028,819
nssv17575105	Remapped	Perfect	NC_000006.11:g.269 05018_26996598dup	GRCh37.p13	First Pass	NC_000006.11	Chr6	26,905,018	26,996,598

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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