A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697536



Internal ID21219385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29556104..29556104hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697536
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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