A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682457



Internal ID21204315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174087492..174087492hg38UCSC Ensembl
chr2:174952220..174952220hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg382426
hg192426
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2805830
Supporting Variants
Samples
Known GenesOLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682457
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.109375


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