A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7986



Internal ID15845898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160606022..160660639hg38UCSC Ensembl
Outerchr6:161027054..161081671hg19UCSC Ensembl
Outerchr6:160947044..161001661hg18UCSC Ensembl
Outerchr6:160997465..161052082hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3854618
hg1954618
hg1854618
hg1754618
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15269, nssv14454, nssv15078, nssv15286, nssv16857, nssv13990, nssv13631, nssv16911, nssv14627, nssv15818, nssv14827, nssv15064, nssv14597, nssv14815, nssv14362, nssv15848, nssv14895, nssv13669, nssv17670, nssv14555, nssv17213, nssv17504, nssv15123, nssv14726
SamplesNA11830, NA18980, NA12155, NA18563, NA12802, NA18860, NA18942, NA07048, NA10839, NA18975, NA19007, NA10847, NA12872, NA18572, NA19221, NA18537, NA19132, NA18517, NA18564, NA19173, NA18972, NA18552
Known GenesLPA
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)nsv7986
Frequency
Sample Size31
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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