A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024932



Internal ID84346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60617355..60617490hg38UCSC Ensembl
chr9_gl000199_random:98797..98932hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486111
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024932
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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