A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364967



Internal ID21022520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85624401..85647800hg38UCSC Ensembl
chr3:85673551..85696950hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3823400
hg1923400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210132
Samples
Known GenesCADM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364967
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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