A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10806



Internal ID15845769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26883163..27003585hg38UCSC Ensembl
Outerchr6:26850942..26971364hg19UCSC Ensembl
Outerchr6:26958921..27079343hg18UCSC Ensembl
Outerchr6:26958921..27079343hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38120423
hg19120423
hg18120423
hg17120423
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14616, nssv14248, nssv14055, nssv15129, nssv15823, nssv15159, nssv15402, nssv14536, nssv14012, nssv16334, nssv14278, nssv16274, nssv16493, nssv14646, nssv13270, nssv16304, nssv15068, nssv13985
SamplesNA18502, NA07029, NA18504, NA12155, NA12802, NA10847, NA10863, NA18537, NA18517, NA19144, NA12740, NA18972, NA18552
Known GenesGUSBP2, LINC00240
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)nsv10806
Frequency
Sample Size31
Observed Gain7
Observed Loss9
Observed Complex0
Frequencyn/a


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