A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207926



Internal ID20774966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120545493..120546080hg38UCSC Ensembl
chr3:120264340..120264927hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373992
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207926
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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