A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5908n223



Internal ID22808876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117678083..117796398hg38UCSC Ensembl
chr5:117013778..117132093hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38118316
hg19118316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6410697, nsv6406108
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5908n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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