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dbVar

Database of genomic structural variation

nsv5922736

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:1,081

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: 171 SVs from 38 studies. See in: genome view

Submitted genomic12,775,028-12,776,108

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5922736	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	12,775,028	12,776,108
nsv5922736	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	12,817,027	12,818,107

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17350855	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17350855	Submitted genomic		NC_000010.11:g.127 75028_12776108del	GRCh38 (hg38)		NC_000010.11	Chr10	12,775,028	12,776,108
nssv17350855	Remapped	Perfect	NC_000010.10:g.128 17027_12818107del	GRCh37.p13	First Pass	NC_000010.10	Chr10	12,817,027	12,818,107

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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