A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702262



Internal ID125928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85291627..85464876hg38UCSC Ensembl
chr15:85834858..86008107hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38173250
hg19173250
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529523
Supporting Variants
Samples
Known GenesAKAP13
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702262
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001874


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