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dbVar

Database of genomic structural variation

nsv5581289

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:4,858

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: 205 SVs from 48 studies. See in: genome view

Submitted genomic132,386,421-132,391,278

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5581289	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	132,386,421	132,391,278
nsv5581289	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	132,707,560	132,712,417

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17141721	deletion	SAMN00801888	Sequencing	Sequence alignment	2,004

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17141721	Submitted genomic		NC_000006.12:g.132 386421_132391278de lA	GRCh38 (hg38)		NC_000006.12	Chr6	132,386,421	132,391,278
nssv17141721	Remapped	Perfect	NC_000006.11:g.132 707560_132712417de lA	GRCh37.p13	First Pass	NC_000006.11	Chr6	132,707,560	132,712,417

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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