A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14668



Internal ID15842714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32569429..32574610hg38UCSC Ensembl
Outerchr6:32568705..32575392hg38UCSC Ensembl
Innerchr6:32537206..32542387hg19UCSC Ensembl
Outerchr6:32536482..32543169hg19UCSC Ensembl
Innerchr6:32645184..32650365hg18UCSC Ensembl
Outerchr6:32644460..32651147hg18UCSC Ensembl
Innerchr6:32645184..32650365hg17UCSC Ensembl
Outerchr6:32644460..32651147hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386688
hg196688
hg186688
hg176688
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7883
Supporting Variants
SamplesNA19144
Known Genes
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)nssv14668
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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