A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024119



Internal ID83801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65910446..65910573hg38UCSC Ensembl
chr9:42610762..42610889hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024119
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004686


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