A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26673



Internal ID15488186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45434478..45438803hg38UCSC Ensembl
Outerchr22:45434049..45441452hg38UCSC Ensembl
Innerchr22:45830358..45834684hg19UCSC Ensembl
Outerchr22:45829929..45837333hg19UCSC Ensembl
Innerchr22:44209022..44213348hg18UCSC Ensembl
Outerchr22:44208593..44215997hg18UCSC Ensembl
Innerchr22:44150895..44155221hg17UCSC Ensembl
Outerchr22:44150466..44157870hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg387404
hg197405
hg187405
hg177405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9921
Supporting Variants
SamplesNA18537
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)nssv26673
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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