A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15158



Internal ID15483824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29975476..29977269hg38UCSC Ensembl
Outerchr6:29974758..29977565hg38UCSC Ensembl
Innerchr6:29943253..29945046hg19UCSC Ensembl
Outerchr6:29942535..29945342hg19UCSC Ensembl
Innerchr6:30051232..30053025hg18UCSC Ensembl
Outerchr6:30050514..30053321hg18UCSC Ensembl
Innerchr6:30051232..30053025hg17UCSC Ensembl
Outerchr6:30050514..30053321hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg382808
hg192808
hg182808
hg172808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10810
Supporting Variants
SamplesNA12155
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)nssv15158
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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