A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9195



Internal ID15847107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:24079653..24549275hg38UCSC Ensembl
Outerchr15:24324800..24794422hg19UCSC Ensembl
Outerchr15:21875893..22345515hg18UCSC Ensembl
Outerchr15:21875893..22345515hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38469623
hg19469623
hg18469623
hg17469623
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25117, nssv23205, nssv25891, nssv22135, nssv27127, nssv25544, nssv19540, nssv25475, nssv22024, nssv23177, nssv21836, nssv25849, nssv25870, nssv21866, nssv22919, nssv21896, nssv23149, nssv19390, nssv22335, nssv21746, nssv22075, nssv20362, nssv25912, nssv21806, nssv25498, nssv21032, nssv25828, nssv25567, nssv22045, nssv19480, nssv25521, nssv21716, nssv25092, nssv19450, nssv21002, nssv19510
SamplesNA18502, NA11830, NA18980, NA07029, NA12155, NA12802, NA18860, NA18942, NA10839, NA19007, NA19221, NA18537, NA18517
Known GenesPWRN2
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)nsv9195
Frequency
Sample Size31
Observed Gain3
Observed Loss12
Observed Complex0
Frequencyn/a


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