A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411746



Internal ID21069299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60682801..60715100hg38UCSC Ensembl
chr5:59978628..60010927hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3832300
hg1932300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216246
Samples
Known GenesDEPDC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411746
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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