A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025731



Internal ID84890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94020901..94045405hg38UCSC Ensembl
chr9:96783183..96807687hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3824505
hg1924505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493891
Supporting Variants
Samples
Known GenesPTPDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025731
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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