A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009404



Internal ID73902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32960927..32971167hg38UCSC Ensembl
chr8:32818445..32828685hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3810241
hg1910241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484880
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009404
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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