A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8628



Internal ID15846540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45674512..45707726hg38UCSC Ensembl
Outerchr10:46169960..46203174hg19UCSC Ensembl
Outerchr10:45489966..45523180hg18UCSC Ensembl
Outerchr10:45489966..45523180hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3833215
hg1933215
hg1833215
hg1733215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23452, nssv18325, nssv17212, nssv17936, nssv20833, nssv20982, nssv21657, nssv19217
SamplesNA18502, NA18980, NA18504, NA18563, NA18942, NA19007, NA19221, NA19132
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)nsv8628
Frequency
Sample Size31
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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