A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13691855



Internal ID21213711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72347197..72347197hg38UCSC Ensembl
chr15:72639538..72639538hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795367
Supporting Variants
Samples
Known GenesHEXA
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13691855
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.693548


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