A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14900



Internal ID15490872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:113279..115995hg18UCSC Ensembl
Outerchr7:113146..116273hg18UCSC Ensembl
Innerchr7:113279..115995hg17UCSC Ensembl
Outerchr7:113146..116273hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg183128
hg173128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8023
Supporting Variants
SamplesNA18853
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)nssv14900
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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