A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360651



Internal ID21018204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:790010..3040518hg38UCSC Ensembl
chr3:831693..3082202hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg382250509
hg192250510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4749n223
Supporting Variantsnssv18209410
Samples
Known GenesCNTN4, CNTN4-AS2, CNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360651
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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