A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25774



Internal ID15830116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64304768..64330090hg38UCSC Ensembl
Outerchr20:64304729..64334167hg38UCSC Ensembl
Innerchr20:62936121..62961443hg19UCSC Ensembl
Outerchr20:62936082..62965520hg19UCSC Ensembl
Innerchr20:62406565..62431887hg18UCSC Ensembl
Outerchr20:62406526..62435964hg18UCSC Ensembl
Innerchr20:62406565..62431887hg17UCSC Ensembl
Outerchr20:62406526..62435964hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3829439
hg1929439
hg1829439
hg1729439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9836
Supporting Variants
SamplesNA11830
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)nssv25774
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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