A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367040



Internal ID21024593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86072801..86075100hg38UCSC Ensembl
chr3:86121951..86124250hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106074
Samples
Known GenesCADM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367040
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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