A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365769



Internal ID21023322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167384263..167396056hg38UCSC Ensembl
chr3:167102051..167113844hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3811794
hg1911794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208585
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365769
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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