A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26267



Internal ID15495810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50054643..50057870hg38UCSC Ensembl
Outerchr19:50052833..50058372hg38UCSC Ensembl
Innerchr19:50557900..50561127hg19UCSC Ensembl
Outerchr19:50556090..50561629hg19UCSC Ensembl
Innerchr19:55249712..55252939hg18UCSC Ensembl
Outerchr19:55247902..55253441hg18UCSC Ensembl
Innerchr19:55249712..55252939hg17UCSC Ensembl
Outerchr19:55247902..55253441hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg385540
hg195540
hg185540
hg175540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9739
Supporting Variants
SamplesNA19144
Known GenesFLJ26850
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)nssv26267
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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