A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9881



Internal ID15847793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:24178619..24186715hg38UCSC Ensembl
Outerchr22:24574587..24582683hg19UCSC Ensembl
Outerchr22:22904587..22912683hg18UCSC Ensembl
Outerchr22:22899141..22907237hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg388097
hg198097
hg188097
hg178097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24778
SamplesNA07029
Known GenesCABIN1, SUSD2
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)nsv9881
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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