A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105980



Internal ID20673020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85503704..85619217hg38UCSC Ensembl
chr3:85552854..85668367hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38115514
hg19115514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364384
Supporting Variants
Samples
Known GenesCADM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105980
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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