A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025732



Internal ID84891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94048705..94052038hg38UCSC Ensembl
chr9:96810987..96814320hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg383334
hg193334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475535
Supporting Variants
Samples
Known GenesPTPDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025732
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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