A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13952



Internal ID15827551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:296581..378926hg38UCSC Ensembl
Outerchr6:295278..379865hg38UCSC Ensembl
Innerchr6:296581..378926hg19UCSC Ensembl
Outerchr6:295278..379865hg19UCSC Ensembl
Innerchr6:241581..323926hg18UCSC Ensembl
Outerchr6:240278..324865hg18UCSC Ensembl
Innerchr6:241581..323926hg17UCSC Ensembl
Outerchr6:240278..324865hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3884588
hg1984588
hg1884588
hg1784588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10799
Supporting Variants
SamplesNA07029
Known GenesDUSP22
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)nssv13952
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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