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dbVar

Database of genomic structural variation

nsv5946943

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:212

Publication(s):Almarri et al. 2020

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: 105 SVs from 24 studies. See in: genome view

Submitted genomic76,035,071-76,035,282

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5946943	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	76,035,071	76,035,282
nsv5946943	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	76,428,851	76,429,062

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17358272	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17358272	Submitted genomic		NC_000012.12:g.760 35071_76035282del	GRCh38 (hg38)		NC_000012.12	Chr12	76,035,071	76,035,282
nssv17358272	Remapped	Perfect	NC_000012.11:g.764 28851_76429062del	GRCh37.p13	First Pass	NC_000012.11	Chr12	76,428,851	76,429,062

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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