A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096247



Internal ID21273375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57557510..57563517hg38UCSC Ensembl
Innerchr15:57849708..57855715hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386008
hg196008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111902
Supporting Variants
Samplessample190
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096247
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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