A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493891



Internal ID271055
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 StatusM
Merged Variants
Supporting Variantsnssv17025731
Samples
Known GenesPTPDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493891
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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