A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364860



Internal ID21022413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5114516..5243418hg38UCSC Ensembl
chr3:5156201..5285103hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38128903
hg19128903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209968
Samples
Known GenesARL8B, EDEM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364860
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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