A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9908



Internal ID15501134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:38990517..38995926hg38UCSC Ensembl
Outerchr22:39386522..39391931hg19UCSC Ensembl
Outerchr22:37716468..37721877hg18UCSC Ensembl
Outerchr22:37711022..37716431hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385410
hg195410
hg185410
hg175410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26621
SamplesNA18537
Known GenesAPOBEC3A_B, APOBEC3B, APOBEC3B-AS1
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)nsv9908
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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