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dbVar

Database of genomic structural variation

nsv5580932

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:153

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: 353 SVs from 69 studies. See in: genome view

Submitted genomic143,859,878-143,860,030

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5580932	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	143,859,878	143,860,030
nsv5580932	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	143,556,971	143,557,123

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17155500	deletion	HG02818	Sequencing	Sequence alignment	3,473

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17155500	Submitted genomic		NC_000007.14:g.143 859878_143860030de lT	GRCh38 (hg38)		NC_000007.14	Chr7	143,859,878	143,860,030
nssv17155500	Remapped	Perfect	NC_000007.13:g.143 556971_143557123de lT	GRCh37.p13	First Pass	NC_000007.13	Chr7	143,556,971	143,557,123

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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