A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16011



Internal ID15491446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29975932..29988780hg38UCSC Ensembl
Outerchr6:29975476..29989306hg38UCSC Ensembl
Innerchr6:29943709..29956557hg19UCSC Ensembl
Outerchr6:29943253..29957083hg19UCSC Ensembl
Innerchr6:30051688..30064536hg18UCSC Ensembl
Outerchr6:30051232..30065062hg18UCSC Ensembl
Innerchr6:30051688..30064536hg17UCSC Ensembl
Outerchr6:30051232..30065062hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3813831
hg1913831
hg1813831
hg1713831
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10810
Supporting Variants
SamplesNA18860
Known GenesHCG9
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)nssv16011
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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