A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210791



Internal ID20777831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9299672..9303325hg38UCSC Ensembl
chr3:9341356..9345009hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg383654
hg193654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368430
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210791
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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