A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8446



Internal ID15846358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:38771899..38964722hg38UCSC Ensembl
Outerchr9:38771896..38964719hg19UCSC Ensembl
Outerchr9:38761896..38954719hg18UCSC Ensembl
Outerchr9:38761896..38954719hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38192824
hg19192824
hg18192824
hg17192824
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv20217, nssv20247, nssv20211, nssv17270, nssv18309, nssv17464, nssv18358, nssv16702, nssv20181, nssv17004, nssv20834, nssv20573, nssv18018, nssv17973, nssv17596, nssv17605, nssv19141, nssv16565, nssv16946, nssv17494, nssv19782, nssv17827, nssv21930, nssv17057, nssv15821
SamplesNA18502, NA11830, NA18980, NA18563, NA18860, NA18942, NA07048, NA10839, NA18975, NA19007, NA10847, NA12872, NA19221, NA18853, NA19132, NA18517, NA18564, NA19240, NA19144, 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)nsv8446
Frequency
Sample Size31
Observed Gain6
Observed Loss17
Observed Complex0
Frequencyn/a


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