A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24861



Internal ID15833691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101906484..101949773hg38UCSC Ensembl
Outerchr15:101906131..101953075hg38UCSC Ensembl
Innerchr15:102446687..102489976hg19UCSC Ensembl
Outerchr15:102446334..102493278hg19UCSC Ensembl
Innerchr15:100264210..100307499hg18UCSC Ensembl
Outerchr15:100263857..100310801hg18UCSC Ensembl
Innerchr15:100264210..100307499hg17UCSC Ensembl
Outerchr15:100263857..100310801hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3846945
hg1946945
hg1846945
hg1746945
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9315
Supporting Variants
SamplesNA18504
Known GenesOR4F4
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)nssv24861
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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