A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21384



Internal ID15840096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28232003..28232631hg38UCSC Ensembl
Outerchr15:28231103..28232987hg38UCSC Ensembl
Innerchr15:28477149..28477777hg19UCSC Ensembl
Outerchr15:28476249..28478133hg19UCSC Ensembl
Innerchr15:26150744..26151372hg18UCSC Ensembl
Outerchr15:26149844..26151728hg18UCSC Ensembl
Innerchr15:26150744..26151372hg17UCSC Ensembl
Outerchr15:26149844..26151728hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381885
hg191885
hg181885
hg171885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9205
Supporting Variants
SamplesNA18975
Known GenesHERC2
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv21384
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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