A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10818



Internal ID15845781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:31354336..31360403hg38UCSC Ensembl
Outerchr6:31322113..31328180hg19UCSC Ensembl
Outerchr6:31430092..31436159hg18UCSC Ensembl
Outerchr6:31430092..31436159hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg386068
hg196068
hg186068
hg176068
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14886, nssv16650
SamplesNA10863, NA19221
Known GenesHLA-B, MIR6891
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)nsv10818
Frequency
Sample Size31
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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