A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690836



Internal ID21212689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62830652..62830652hg38UCSC Ensembl
chr20:61462004..61462004hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802773
Supporting Variants
Samples
Known GenesCOL9A3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690836
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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