A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362747



Internal ID21020300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119970906..119975465hg38UCSC Ensembl
chr3:119689753..119694312hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg384560
hg194560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207920
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362747
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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