A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14020



Internal ID15831680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160754539..160754968hg38UCSC Ensembl
Outerchr6:160754160..160755618hg38UCSC Ensembl
Innerchr6:161175571..161176000hg19UCSC Ensembl
Outerchr6:161175192..161176650hg19UCSC Ensembl
Innerchr6:161095561..161095990hg18UCSC Ensembl
Outerchr6:161095182..161096640hg18UCSC Ensembl
Innerchr6:161145982..161146411hg17UCSC Ensembl
Outerchr6:161145603..161147061hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381459
hg191459
hg181459
hg171459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7987
Supporting Variants
SamplesNA12802
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)nssv14020
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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