A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23590



Internal ID15496159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34562688..34578112hg38UCSC Ensembl
Outerchr15:34561072..34578821hg38UCSC Ensembl
Innerchr15:34854889..34870313hg19UCSC Ensembl
Outerchr15:34853273..34871022hg19UCSC Ensembl
Innerchr15:32642181..32657605hg18UCSC Ensembl
Outerchr15:32640565..32658314hg18UCSC Ensembl
Innerchr15:32642181..32657605hg17UCSC Ensembl
Outerchr15:32640565..32658314hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3817750
hg1917750
hg1817750
hg1717750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA19144
Known GenesGOLGA8B
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)nssv23590
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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