A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14556



Internal ID15482717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10468606..10530414hg38UCSC Ensembl
Outerchr6:10466007..10531236hg38UCSC Ensembl
Innerchr6:10468839..10530647hg19UCSC Ensembl
Outerchr6:10466240..10531469hg19UCSC Ensembl
Innerchr6:10576825..10638633hg18UCSC Ensembl
Outerchr6:10574226..10639455hg18UCSC Ensembl
Innerchr6:10576825..10638633hg17UCSC 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 StatusS
Merged Variantsnsv10801
Supporting Variants
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)nssv14556
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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