A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5960n223



Internal ID22808928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140716001..140726100hg38UCSC Ensembl
chr5:140095586..140105685hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3810100
hg1910100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6411821, nsv6401243
Samples
Known GenesVTRNA1-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5960n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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