A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26223



Internal ID15835140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15869674..15877205hg38UCSC Ensembl
Outerchr22:15869607..15877693hg38UCSC Ensembl
Innerchr22:16100758..16108289hg19UCSC Ensembl
Outerchr22:16100270..16108356hg19UCSC Ensembl
Innerchr22:14480758..14488289hg18UCSC Ensembl
Outerchr22:14480270..14488356hg18UCSC Ensembl
Innerchr22:14480758..14488289hg17UCSC Ensembl
Outerchr22:14480270..14488356hg17UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg388087
hg198087
hg188087
hg178087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9866
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)nssv26223
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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