A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373526



Internal ID21031079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33405488..33407651hg38UCSC Ensembl
chr3:33446980..33449143hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg382164
hg192164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210538
Samples
Known GenesUBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373526
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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