A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210064



Internal ID20777104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82251501..82259900hg38UCSC Ensembl
chr3:82300652..82309051hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368194
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210064
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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