A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025883



Internal ID84992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65521123..65587123hg38UCSC Ensembl
chr9:44797858..44863956hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3866001
hg1966099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486836
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025883
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02282


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