A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17011198



Internal ID75113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29613663..29615128hg38UCSC Ensembl
chr8:29471179..29472644hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381466
hg191466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17011198
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.016547


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