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dbVar

Database of genomic structural variation

nsv5931193

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:842

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: 270 SVs from 23 studies. See in: genome view

Submitted genomic59,462,499-59,463,340

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5931193	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	59,462,499	59,463,340
nsv5931193	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	57,129,731	57,130,572

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17369752	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17369752	Submitted genomic		NC_000018.10:g.594 62499_59463340del	GRCh38 (hg38)		NC_000018.10	Chr18	59,462,499	59,463,340
nssv17369752	Remapped	Perfect	NC_000018.9:g.5712 9731_57130572del	GRCh37.p13	First Pass	NC_000018.9	Chr18	57,129,731	57,130,572

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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