A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367934



Internal ID21025487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85628005..85628481hg38UCSC Ensembl
chr3:85677155..85677631hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210133
Samples
Known GenesCADM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367934
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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