A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738477



Internal ID162143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72163140..72163276hg38UCSC Ensembl
chr9:74778056..74778192hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483069
Supporting Variants
Samples
Known GenesGDA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738477
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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