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dbVar

Database of genomic structural variation

nsv5591057

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:260

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: 1889 SVs from 78 studies. See in: genome view

Submitted genomic47,580,847-47,581,106

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5591057	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	47,580,847	47,581,106
nsv5591057	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_003871068.1	Chr10\|NW_0 03871068.1	1,851,962	1,852,221

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17070764	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
nssv17070764	Submitted genomic		NC_000010.11:g.475 80847_47581106delG	GRCh38 (hg38)		NC_000010.11	Chr10	47,580,847	47,581,106
nssv17070764	Remapped	Perfect	NW_003871068.1:g.1 851962_1852221delG	GRCh37.p13	First Pass	NW_003871068.1	Chr10\|NW_0 03871068.1	1,851,962	1,852,221

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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