A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17804



Internal ID15487543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:113279..116273hg18UCSC Ensembl
Outerchr7:113146..116290hg18UCSC Ensembl
Innerchr7:113279..116273hg17UCSC Ensembl
Outerchr7:113146..116290hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg183145
hg173145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8023
Supporting Variants
SamplesNA18517
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)nssv17804
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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