A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678356



Internal ID21200213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61989080..61989080hg38UCSC Ensembl
chr15:62281279..62281279hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794978
Supporting Variants
Samples
Known GenesVPS13C
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678356
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03125


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