A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166637



Internal ID20733677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33560501..33562800hg38UCSC Ensembl
chr8:33418019..33420318hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429596
Supporting Variants
Samples
Known GenesRNF122
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00267


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