A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7901



Internal ID15845813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:54049693..54116282hg38UCSC Ensembl
Outerchr6:53914491..53981080hg19UCSC Ensembl
Outerchr6:54022450..54089039hg18UCSC Ensembl
Outerchr6:54022450..54089039hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3866590
hg1966590
hg1866590
hg1766590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330, nssv14969, nssv14305, nssv14794, nssv16793, nssv16521, nssv13399, nssv16467, nssv17114, nssv13600, nssv14587, nssv16483, nssv15912, nssv14968, nssv14357, nssv17220, nssv15421, nssv15638, nssv13972, nssv14956, nssv15186, nssv14396, nssv14342
SamplesNA18502, NA11830, NA18980, NA07029, NA18504, NA12155, NA18563, NA12802, NA18860, NA18942, NA10839, NA19007, NA10863, NA18572, NA19221, NA18853, NA19132, NA18517, NA19240, NA19144, NA19173, NA18972, NA18552
Known GenesMLIP
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)nsv7901
Frequency
Sample Size31
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer