A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690901



Internal ID21212754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:407966..407966hg38UCSC Ensembl
chr20:388610..388610hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690901
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.666667


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