A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14879



Internal ID15496461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35529493..35598070hg38UCSC Ensembl
Outerchr6:35527726..35598611hg38UCSC Ensembl
Innerchr6:35497270..35565847hg19UCSC Ensembl
Outerchr6:35495503..35566388hg19UCSC Ensembl
Innerchr6:35605248..35673825hg18UCSC Ensembl
Outerchr6:35603481..35674366hg18UCSC Ensembl
Innerchr6:35605248..35673825hg17UCSC Ensembl
Outerchr6:35603481..35674366hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3870886
hg1970886
hg1870886
hg1770886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7889
Supporting Variants
SamplesNA19173
Known GenesFKBP5
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)nssv14879
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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