A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26085



Internal ID15841430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:34899334..34901996hg38UCSC Ensembl
Outerchr22:34898394..34902097hg38UCSC Ensembl
Innerchr22:35295325..35297987hg19UCSC Ensembl
Outerchr22:35294385..35298088hg19UCSC Ensembl
Innerchr22:33625325..33627987hg18UCSC Ensembl
Outerchr22:33624385..33628088hg18UCSC Ensembl
Innerchr22:33619879..33622541hg17UCSC Ensembl
Outerchr22:33618939..33622642hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg383704
hg193704
hg183704
hg173704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9898
Supporting Variants
SamplesNA19007
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)nssv26085
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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