A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413502



Internal ID21071055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54020402..54032786hg38UCSC Ensembl
chr5:53316232..53328616hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3812385
hg1912385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214024
Samples
Known GenesARL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413502
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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