A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194026



Internal ID20761066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76977306..77105587hg38UCSC Ensembl
chr13:77551441..77679722hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38128282
hg19128282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494197
Supporting Variants
Samples
Known GenesCLN5, FBXL3, MYCBP2, MYCBP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194026
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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