A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383255



Internal ID21040808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43386341..43387896hg38UCSC Ensembl
chr5:43386443..43387998hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg381556
hg191556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130517
Samples
Known GenesCCL28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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