A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210517



Internal ID20777557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31859908..32260156hg38UCSC Ensembl
chr3:31901400..32301648hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38400249
hg19400249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360563
Supporting Variants
Samples
Known GenesCMTM8, GPD1L, OSBPL10, ZNF860
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210517
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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