A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679161



Internal ID21201023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61273529..61273529hg38UCSC Ensembl
chr20:59848585..59848585hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803558
Supporting Variants
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679161
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.979167


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