A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210534



Internal ID20777574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33086301..33293000hg38UCSC Ensembl
chr3:33127793..33334492hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38206700
hg19206700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371270
Supporting Variants
Samples
Known GenesCRTAP, FBXL2, GLB1, SUSD5, TMPPE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00082


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