A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689020



Internal ID21210876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63942345..63942345hg38UCSC Ensembl
chr20:62573698..62573698hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803617
Supporting Variants
Samples
Known GenesUCKL1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689020
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.2


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