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dbVar

Database of genomic structural variation

nsv5584848

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:2,977

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: 125 SVs from 44 studies. See in: genome view

Submitted genomic71,501,699-71,504,675

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5584848	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	71,501,699	71,504,675
nsv5584848	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	71,212,745	71,215,721

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17075953	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
nssv17075953	Submitted genomic		NC_000011.10:g.715 01699_71504675delG	GRCh38 (hg38)		NC_000011.10	Chr11	71,501,699	71,504,675
nssv17075953	Remapped	Perfect	NC_000011.9:g.7121 2745_71215721delG	GRCh37.p13	First Pass	NC_000011.9	Chr11	71,212,745	71,215,721

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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