A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193074



Internal ID20760114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:65181713..65217320hg38UCSC Ensembl
chr13:65755845..65791452hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3835608
hg1935608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193074
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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