A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367257



Internal ID21024810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179245848..179333436hg38UCSC Ensembl
chr3:178963636..179051224hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3887589
hg1987589
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211513
Samples
Known GenesKCNMB3, ZNF639
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367257
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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