A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14060



Internal ID15837615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32515648..32516141hg38UCSC Ensembl
Outerchr6:32515331..32517069hg38UCSC Ensembl
Innerchr6:32483425..32483918hg19UCSC Ensembl
Outerchr6:32483108..32484846hg19UCSC Ensembl
Innerchr6:32591403..32591896hg18UCSC Ensembl
Outerchr6:32591086..32592824hg18UCSC Ensembl
Innerchr6:32591403..32591896hg17UCSC Ensembl
Outerchr6:32591086..32592824hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381739
hg191739
hg181739
hg171739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7883
Supporting Variants
SamplesNA18853
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)nssv14060
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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