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dbVar

Database of genomic structural variation

nsv5584617

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:1,711

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: 406 SVs from 58 studies. See in: genome view

Submitted genomic61,855,360-61,857,070

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5584617	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	61,855,360	61,857,070
nsv5584617	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	44,991,512	44,993,222

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17162559	deletion	HG00514	Sequencing	Sequence alignment	257

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17162559	Submitted genomic		NC_000009.12:g.618 55360_61857070delT	GRCh38 (hg38)		NC_000009.12	Chr9	61,855,360	61,857,070
nssv17162559	Remapped	Perfect	NC_000009.11:g.449 91512_44993222delT	GRCh37.p13	First Pass	NC_000009.11	Chr9	44,991,512	44,993,222

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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