A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25257



Internal ID15841222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51594232..51600998hg38UCSC Ensembl
Outerchr19:51593613..51601398hg38UCSC Ensembl
Innerchr19:52097485..52104251hg19UCSC Ensembl
Outerchr19:52096866..52104651hg19UCSC Ensembl
Innerchr19:56789297..56796063hg18UCSC Ensembl
Outerchr19:56788678..56796463hg18UCSC Ensembl
Innerchr19:56789297..56796063hg17UCSC Ensembl
Outerchr19:56788678..56796463hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg387786
hg197786
hg187786
hg177786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9740
Supporting Variants
SamplesNA19007
Known GenesFLJ30403
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)nssv25257
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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