A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25658



Internal ID15484373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47907318..47957242hg38UCSC Ensembl
Outerchr19:47906236..47957278hg38UCSC Ensembl
Innerchr19:48410575..48460499hg19UCSC Ensembl
Outerchr19:48409493..48460535hg19UCSC Ensembl
Innerchr19:53102387..53152311hg18UCSC Ensembl
Outerchr19:53101305..53152347hg18UCSC Ensembl
Innerchr19:53102387..53152311hg17UCSC Ensembl
Outerchr19:53101305..53152347hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3851043
hg1951043
hg1851043
hg1751043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9739
Supporting Variants
SamplesNA12740
Known GenesSNAR-A1, SNAR-A10, SNAR-A11, SNAR-A12, SNAR-A13, SNAR-A14, SNAR-A2, SNAR-A3, SNAR-A4, SNAR-A5, SNAR-A6, SNAR-A7, SNAR-A8, SNAR-A9, SNAR-C1, SNAR-C2, SNAR-C3, SNAR-C4, SNAR-C5
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)nssv25658
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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