A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27466



Internal ID15493103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23035789..23039515hg38UCSC Ensembl
Outerchr19:23016322..23040826hg38UCSC Ensembl
Innerchr19:23218591..23222317hg19UCSC Ensembl
Outerchr19:23199124..23223628hg19UCSC Ensembl
Innerchr19:23010431..23014157hg18UCSC Ensembl
Outerchr19:22990964..23015468hg18UCSC Ensembl
Innerchr19:23010431..23014157hg17UCSC Ensembl
Outerchr19:22990964..23015468hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3824505
hg1924505
hg1824505
hg1724505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9686
Supporting Variants
SamplesNA18972
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)nssv27466
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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