A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13309



Internal ID15837180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32680910..32684833hg38UCSC Ensembl
Outerchr6:32669966..32685264hg38UCSC Ensembl
Innerchr6:32648687..32652610hg19UCSC Ensembl
Outerchr6:32637743..32653041hg19UCSC Ensembl
Innerchr6:32756665..32760588hg18UCSC Ensembl
Outerchr6:32745721..32761019hg18UCSC Ensembl
Innerchr6:32756665..32760588hg17UCSC Ensembl
Outerchr6:32745721..32761019hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3815299
hg1915299
hg1815299
hg1715299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7883
Supporting Variants
SamplesNA18572
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)nssv13309
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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