A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25281



Internal ID15493752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23035789..23041028hg38UCSC Ensembl
Outerchr19:23016322..23041769hg38UCSC Ensembl
Innerchr19:23218591..23223830hg19UCSC Ensembl
Outerchr19:23199124..23224571hg19UCSC Ensembl
Innerchr19:23010431..23015670hg18UCSC Ensembl
Outerchr19:22990964..23016411hg18UCSC Ensembl
Innerchr19:23010431..23015670hg17UCSC Ensembl
Outerchr19:22990964..23016411hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3825448
hg1925448
hg1825448
hg1725448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9686
Supporting Variants
SamplesNA18980
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)nssv25281
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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