A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14276



Internal ID15841306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32635960..32667823hg38UCSC Ensembl
Outerchr6:32634699..32668795hg38UCSC Ensembl
Innerchr6:32603737..32635600hg19UCSC Ensembl
Outerchr6:32602476..32636572hg19UCSC Ensembl
Innerchr6:32711715..32743578hg18UCSC Ensembl
Outerchr6:32710454..32744550hg18UCSC Ensembl
Innerchr6:32711715..32743578hg17UCSC Ensembl
Outerchr6:32710454..32744550hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3834097
hg1934097
hg1834097
hg1734097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7883
Supporting Variants
SamplesNA19007
Known GenesHLA-DQA1, HLA-DQB1
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)nssv14276
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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