A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368769



Internal ID21026322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167102801..167142000hg38UCSC Ensembl
chr3:166820589..166859788hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3839200
hg1939200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368769
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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