A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009436



Internal ID73927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33258733..33258927hg38UCSC Ensembl
chr8:33116251..33116445hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009436
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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