A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097202



Internal ID21284650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67820898..67830202hg38UCSC Ensembl
Innerchr15:68113236..68122540hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg389305
hg199305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114857
Supporting Variants
Samplessample363
Known GenesSKOR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097202
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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