A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26800



Internal ID15498219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22958935..22959467hg38UCSC Ensembl
Outerchr19:22943557..22960331hg38UCSC Ensembl
Innerchr19:23141737..23142269hg19UCSC Ensembl
Outerchr19:23126359..23143133hg19UCSC Ensembl
Innerchr19:22933577..22934109hg18UCSC Ensembl
Outerchr19:22918199..22934973hg18UCSC Ensembl
Innerchr19:22933577..22934109hg17UCSC Ensembl
Outerchr19:22918199..22934973hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3816775
hg1916775
hg1816775
hg1716775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9686
Supporting Variants
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)nssv26800
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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