A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27187



Internal ID15843503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28216850..28218475hg38UCSC Ensembl
Outerchr15:28216256..28218714hg38UCSC Ensembl
Innerchr15:28461996..28463621hg19UCSC Ensembl
Outerchr15:28461402..28463860hg19UCSC Ensembl
Innerchr15:26135591..26137216hg18UCSC Ensembl
Outerchr15:26134997..26137455hg18UCSC Ensembl
Innerchr15:26135591..26137216hg17UCSC Ensembl
Outerchr15:26134997..26137455hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382459
hg192459
hg182459
hg172459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9205
Supporting Variants
SamplesNA19221
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)nssv27187
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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