A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8226



Internal ID15846138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:142786341..142797721hg38UCSC Ensembl
Outerchr7:142194153..142205533hg18UCSC Ensembl
Outerchr7:142000868..142012248hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3811381
hg1811381
hg1711381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16593
SamplesNA07048
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)nsv8226
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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