A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694113



Internal ID117779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98277922..98277934hg38UCSC Ensembl
chr13:98930176..98930188hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551666
Supporting Variants
Samples
Known GenesFARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694113
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.048351


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