A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035965



Internal ID91723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64607916..65086250hg38UCSC Ensembl
chr10:66367673..66846008hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38478335
hg19478336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487125
Supporting Variants
Samples
Known GenesANXA2P3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035965
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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