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dbVar

Database of genomic structural variation

nsv5584439

Organism: Homo sapiens

Study:nstd207 (Ebert 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:69,305

Publication(s):Ebert 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: 2629 SVs from 99 studies. See in: genome view

Submitted genomic78,257,453-78,326,757

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5584439	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	78,257,453	78,326,757
nsv5584439	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	78,967,170	79,036,474

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17155497	deletion	HG03065	Sequencing	Sequence alignment	3,836

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17155497	Submitted genomic		NC_000006.12:g.782 57453_78326757delT	GRCh38 (hg38)		NC_000006.12	Chr6	78,257,453	78,326,757
nssv17155497	Remapped	Perfect	NC_000006.11:g.789 67170_79036474delT	GRCh37.p13	First Pass	NC_000006.11	Chr6	78,967,170	79,036,474

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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