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dbVar

Database of genomic structural variation

nsv6006467

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:138,040

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: 490 SVs from 65 studies. See in: genome view

Submitted genomic49,432,367-49,570,406

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6006467	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	49,432,367	49,570,406
nsv6006467	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	49,400,080	49,538,119

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17577019	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17577019	Submitted genomic		NC_000006.12:g.494 32367_49570406dup	GRCh38 (hg38)		NC_000006.12	Chr6	49,432,367	49,570,406
nssv17577019	Remapped	Perfect	NC_000006.11:g.494 00080_49538119dup	GRCh37.p13	First Pass	NC_000006.11	Chr6	49,400,080	49,538,119

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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