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dbVar

Database of genomic structural variation

nsv5589992

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:138

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: 103 SVs from 31 studies. See in: genome view

Submitted genomic111,595,797-111,595,934

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5589992	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	111,595,797	111,595,934
nsv5589992	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	112,033,601	112,033,738

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17077188	deletion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17077188	Submitted genomic		NC_000012.12:g.111 595797_111595934de lT	GRCh38 (hg38)		NC_000012.12	Chr12	111,595,797	111,595,934
nssv17077188	Remapped	Perfect	NC_000012.11:g.112 033601_112033738de lT	GRCh37.p13	First Pass	NC_000012.11	Chr12	112,033,601	112,033,738

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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