A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13695264



Internal ID21217112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115664231..115664231hg38UCSC Ensembl
chr3:115383078..115383078hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806757
Supporting Variants
Samples
Known GenesGAP43
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13695264
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.046875


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