A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024133



Internal ID83814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66147191..66172191hg38UCSC Ensembl
chr9:42349159..42374075hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3825001
hg1924917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142272
Supporting Variants
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024133
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.443031


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