A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366435



Internal ID21023988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128574551..128575071hg38UCSC Ensembl
chr3:128293394..128293914hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208487
Samples
Known GenesC3orf27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366435
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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