A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368522



Internal ID21026075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160223801..160226500hg38UCSC Ensembl
chr3:159941588..159944287hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207981
Samples
Known GenesC3orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368522
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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