A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9792



Internal ID15501018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:22343833..22350229hg38UCSC Ensembl
Outerchr20:22324471..22330867hg19UCSC Ensembl
Outerchr20:22272471..22278867hg18UCSC Ensembl
Outerchr20:22272471..22278867hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg386397
hg196397
hg186397
hg176397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26126, nssv25022
SamplesNA18853, NA19173
Known Genes
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)nsv9792
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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