A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096813



Internal ID21289371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:24550925..24572210hg38UCSC Ensembl
Innerchr5:24551034..24572319hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3821286
hg1921286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110850
Supporting Variants
Samplessample46
Known GenesCDH10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096813
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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