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dbVar

Database of genomic structural variation

nsv5926617

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:226

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: 338 SVs from 40 studies. See in: genome view

Submitted genomic132,124,339-132,124,564

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5926617	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	132,124,339	132,124,564
nsv5926617	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	133,937,843	133,938,068

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17355480	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17355480	Submitted genomic		NC_000010.11:g.132 124339_132124564de l	GRCh38 (hg38)		NC_000010.11	Chr10	132,124,339	132,124,564
nssv17355480	Remapped	Perfect	NC_000010.10:g.133 937843_133938068de l	GRCh37.p13	First Pass	NC_000010.10	Chr10	133,937,843	133,938,068

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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