A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030006



Internal ID87724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132713646..132865373hg38UCSC Ensembl
chr9:135589033..135740760hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38151728
hg19151728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476317
Supporting Variants
Samples
Known GenesAK8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030006
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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