A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8403



Internal ID15846315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62805..324255hg38UCSC Ensembl
Outerchr9:62805..324255hg19UCSC Ensembl
Outerchr9:52805..314255hg18UCSC Ensembl
Outerchr9:52805..314255hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38261451
hg19261451
hg18261451
hg17261451
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16369, nssv16856, nssv15671, nssv18238, nssv16339, nssv20393, nssv16967, nssv17515, nssv19021, nssv18578, nssv16884, nssv17856, nssv16505, nssv20654, nssv17192, nssv16582, nssv17506
SamplesNA18980, NA07029, NA12155, NA18563, NA18942, NA18975, NA19007, NA10847, NA10863, NA12872, NA18572, NA18517, NA19240, NA19144, NA18972, NA18552
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
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)nsv8403
Frequency
Sample Size31
Observed Gain8
Observed Loss8
Observed Complex0
Frequencyn/a


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