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dbVar

Database of genomic structural variation

nsv5250774

Organism: Homo sapiens

Study:nstd204 (Chen 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:410,100

Publication(s):Chen 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: 1972 SVs from 93 studies. See in: genome view

Submitted genomic129,443,501-129,853,600

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5250774	Submitted genomic		GRCh38.p13	Primary Assembly		NC_000009.12	Chr9	129,443,501	129,853,600
nsv5250774	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	132,205,780	132,615,879

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16860533	copy number variation	Sequencing	Read depth

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16860533	Submitted genomic		GRCh38.p13		NC_000009.12	Chr9	129,443,501	129,853,600
nssv16860533	Remapped	Perfect	GRCh37.p13	First Pass	NC_000009.11	Chr9	132,205,780	132,615,879

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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