A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8298



Internal ID15499524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:14772387..15806223hg38UCSC Ensembl
Outerchr8:14629896..15663732hg19UCSC Ensembl
Outerchr8:14674267..15708103hg18UCSC Ensembl
Outerchr8:14674267..15708103hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381033837
hg191033837
hg181033837
hg171033837
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15491, nssv17496, nssv19913, nssv18128, nssv16954, nssv19377, nssv20970, nssv19347, nssv19401
SamplesNA12155, NA18860, NA10839, NA10863, NA12872, NA19221, NA19132, NA18972
Known GenesMIR383, SGCZ, TUSC3
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)nsv8298
Frequency
Sample Size31
Observed Gain2
Observed Loss7
Observed Complex0
Frequencyn/a


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