A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13153



Internal ID15833844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26443816..26452257hg38UCSC Ensembl
Outerchr4:26440642..26453160hg38UCSC Ensembl
Innerchr4:26445438..26453879hg19UCSC Ensembl
Outerchr4:26442264..26454782hg19UCSC Ensembl
Innerchr4:26054536..26062977hg18UCSC Ensembl
Outerchr4:26051362..26063880hg18UCSC Ensembl
Innerchr4:26121707..26130148hg17UCSC Ensembl
Outerchr4:26118533..26131051hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3812519
hg1912519
hg1812519
hg1712519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10467
Supporting Variants
SamplesNA18504
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)nssv13153
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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