A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10801



Internal ID15499078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:10466007..10531236hg38UCSC Ensembl
Outerchr6:10466240..10531469hg19UCSC Ensembl
Outerchr6:10574226..10639455hg18UCSC Ensembl
Outerchr6:10574226..10639455hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3865230
hg1965230
hg1865230
hg1765230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14556
SamplesNA10863
Known GenesGCNT2
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)nsv10801
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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