A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682406



Internal ID21204266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58726582..58726582hg38UCSC Ensembl
chr17:56803943..56803943hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2798019
Supporting Variants
Samples
Known GenesRAD51C
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682406
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.609375


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