A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365106



Internal ID21022659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185799711..185804391hg38UCSC Ensembl
chr3:185517499..185522179hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg384681
hg194681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212194
Samples
Known GenesIGF2BP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365106
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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