A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365709



Internal ID21023262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32815801..32818200hg38UCSC Ensembl
chr3:32857293..32859692hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210529
Samples
Known GenesTRIM71
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365709
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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