A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362870



Internal ID21020423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109653958..109670567hg38UCSC Ensembl
chr3:109372805..109389414hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3816610
hg1916610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362870
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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