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dbVar

Database of genomic structural variation

nsv5587435

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:64,810

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: 620 SVs from 60 studies. See in: genome view

Submitted genomic19,145,057-19,209,866

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5587435	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	19,145,057	19,209,866
nsv5587435	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	19,145,055	19,209,864

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17161394	deletion	HG02587	Sequencing	Sequence alignment	2,330

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17161394	Submitted genomic		NC_000009.12:g.191 45057_19209866delT	GRCh38 (hg38)		NC_000009.12	Chr9	19,145,057	19,209,866
nssv17161394	Remapped	Perfect	NC_000009.11:g.191 45055_19209864delT	GRCh37.p13	First Pass	NC_000009.11	Chr9	19,145,055	19,209,864

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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