A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039773



Internal ID94235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97642271..97643457hg38UCSC Ensembl
chr10:99402028..99403214hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381187
hg191187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477295
Supporting Variants
Samples
Known GenesPI4K2A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039773
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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