A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25022



Internal ID15490990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:22345810..22348852hg38UCSC Ensembl
Outerchr20:22343833..22350229hg38UCSC Ensembl
Innerchr20:22326448..22329490hg19UCSC Ensembl
Outerchr20:22324471..22330867hg19UCSC Ensembl
Innerchr20:22274448..22277490hg18UCSC Ensembl
Outerchr20:22272471..22278867hg18UCSC Ensembl
Innerchr20:22274448..22277490hg17UCSC 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 StatusS
Merged Variantsnsv9792
Supporting Variants
SamplesNA18853
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)nssv25022
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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