A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035121



Internal ID91149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69354132..69354602hg38UCSC Ensembl
chr10:71113888..71114358hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476366
Supporting Variants
Samples
Known GenesHK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035121
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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