A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10821



Internal ID15499098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:31485484..31508705hg38UCSC Ensembl
Outerchr6:31453261..31476482hg19UCSC Ensembl
Outerchr6:31561240..31584461hg18UCSC Ensembl
Outerchr6:31561240..31584461hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3823222
hg1923222
hg1823222
hg1723222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13967
SamplesNA18563
Known GenesMICB
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)nsv10821
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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