A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189322



Internal ID20756362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34266739..34268124hg38UCSC Ensembl
chr13:34840876..34842261hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg381386
hg191386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492836
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189322
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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