A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8499



Internal ID15846411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:61996785..62149738hg38UCSC Ensembl
Outerchr9:65957144..66149539hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38152954
hg17192396
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv20161, nssv18198, nssv20472, nssv18487, nssv16301, nssv22797, nssv20871, nssv21503, nssv17002, nssv18639, nssv20442, nssv17930, nssv18046, nssv21327, nssv17516, nssv20131, nssv21164, nssv18633, nssv21297, nssv17704, nssv20841, nssv16775, nssv18345, nssv17905
SamplesNA18502, NA11830, NA18980, NA18860, NA18942, NA07048, NA10839, NA19007, NA10847, NA12872, NA19221, NA18537, NA18853, NA19132, NA18517, NA18564, NA19240, NA12740, NA18972, NA18552
Known Genes
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)nsv8499
Frequency
Sample Size31
Observed Gain8
Observed Loss14
Observed Complex0
Frequencyn/a


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