A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13691632



Internal ID21213484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:121816..121816hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796792
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13691632
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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