A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24406



Internal ID15844546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28590498..28654204hg38UCSC Ensembl
Outerchr15:28590109..28654235hg38UCSC Ensembl
Innerchr15:28835644..28899350hg19UCSC Ensembl
Outerchr15:28835255..28899381hg19UCSC Ensembl
Innerchr15:26634685..26698391hg18UCSC Ensembl
Outerchr15:26634296..26698422hg18UCSC Ensembl
Innerchr15:26634685..26698391hg17UCSC Ensembl
Outerchr15:26634296..26698422hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3864127
hg1964127
hg1864127
hg1764127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9216
Supporting Variants
SamplesNA19240
Known Genes
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)nssv24406
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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