A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10537



Internal ID15845500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:95836420..96035143hg38UCSC Ensembl
Outerchr4:96757571..96956294hg19UCSC Ensembl
Outerchr4:96976594..97175317hg18UCSC Ensembl
Outerchr4:97114749..97313472hg17UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38198724
hg19198724
hg18198724
hg17198724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv12328
SamplesNA19144
Known GenesPDHA2
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)nsv10537
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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