A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13694917



Internal ID21216765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158245132..158245132hg38UCSC Ensembl
chr3:157962921..157962921hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807967
Supporting Variants
Samples
Known GenesRSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13694917
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0833333


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