A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5893n223



Internal ID22808861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112602701..112610100hg38UCSC Ensembl
chr5:111938398..111945797hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6409748, nsv6408001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5893n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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