A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10361



Internal ID15498638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:89010060..89013363hg38UCSC Ensembl
Outerchr1:89475743..89479046hg19UCSC Ensembl
Outerchr1:89248331..89251634hg18UCSC Ensembl
Outerchr1:89187764..89191067hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg383304
hg193304
hg183304
hg173304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14402, nssv16101, nssv12425, nssv19084, nssv14408, nssv14426, nssv15767, nssv17760, nssv14761, nssv12775, nssv13087, nssv14750, nssv13437, nssv13421, nssv17744, nssv16092, nssv14424, nssv17748, nssv15106, nssv14758, nssv15093, nssv13432, nssv16753, nssv14736, nssv20423, nssv17429
SamplesNA18975, NA19173, NA10839, NA10847, NA18972, NA18517, NA19144, NA18860, NA07029, NA10863, NA12155, NA18563, NA07048, NA18502, NA12872, NA18504, NA18564, NA18942, NA19221, NA18552, NA19132, NA11830, NA19240, NA18853, NA19007, NA18980
Known GenesGBP3
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)nsv10361
Frequency
Sample Size31
Observed Gain26
Observed Loss0
Observed Complex0
Frequencyn/a


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