A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13691220



Internal ID21213073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174087492..174087492hg38UCSC Ensembl
chr2:174952220..174952220hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg382669
hg192669
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)nssv13691220
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.109375


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