A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698729



Internal ID21220579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149875898..149875898hg38UCSC Ensembl
chr3:149593685..149593685hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2808440
Supporting Variants
Samples
Known GenesRNF13
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698729
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.921875


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