A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212239



Internal ID20779279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188973828..188991666hg38UCSC Ensembl
chr3:188691617..188709455hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3817839
hg1917839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374523
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212239
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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