A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692759



Internal ID116425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112014938..112015034hg38UCSC Ensembl
chr13:112669252..112669348hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499995
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692759
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.148943


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