A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682109



Internal ID21203969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65581275..65581442hg38UCSC Ensembl
chr15:65873613..65873780hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795270
Supporting Variants
Samples
Known GenesVWA9
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682109
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.133333


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