A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8578



Internal ID15846490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:135165012..135327327hg38UCSC Ensembl
Outerchr9:138056858..138219173hg19UCSC Ensembl
Outerchr9:137196679..137358994hg18UCSC Ensembl
Outerchr9:135282803..135445118hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38162316
hg19162316
hg18162316
hg17162316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18316, nssv21743, nssv18408, nssv18977, nssv18607, nssv17122, nssv16835, nssv17974, nssv20068, nssv16481, nssv18879, nssv19388, nssv21291, nssv18636, nssv18873, nssv18585, nssv16669, nssv16810, nssv17696
SamplesNA11830, NA12155, NA18563, NA12802, NA18860, NA18942, NA07048, NA10839, NA19007, NA10847, NA10863, NA12872, NA18572, NA18537, NA18564, NA19144, NA12740, NA18972, NA18552
Known GenesLOC401557
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)nsv8578
Frequency
Sample Size31
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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