A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097545



Internal ID21274898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60590634..60593971hg38UCSC Ensembl
Innerchr15:60882833..60886170hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg383338
hg193338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111100
Supporting Variants
Samplessample214
Known GenesRORA
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097545
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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