A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703609



Internal ID21225419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23700283..23700283hg38UCSC Ensembl
chr14:24169492..24169492hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794317
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703609
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.34375


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