A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360563



Internal ID21018116
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 StatusM
Merged Variants
Supporting Variantsnssv18210517
Samples
Known GenesCMTM8, GPD1L, OSBPL10, ZNF860
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360563
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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