A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10773



Internal ID15845736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:172574910..172577099hg38UCSC Ensembl
Outerchr5:172001913..172004102hg19UCSC Ensembl
Outerchr5:171934518..171936707hg18UCSC Ensembl
Outerchr5:171934518..171936707hg17UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg382190
hg192190
hg182190
hg172190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14911
SamplesNA19240
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)nsv10773
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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