A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24120



Internal ID15482677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23035789..23038883hg38UCSC Ensembl
Outerchr19:23016322..23039515hg38UCSC Ensembl
Innerchr19:23218591..23221685hg19UCSC Ensembl
Outerchr19:23199124..23222317hg19UCSC Ensembl
Innerchr19:23010431..23013525hg18UCSC Ensembl
Outerchr19:22990964..23014157hg18UCSC Ensembl
Innerchr19:23010431..23013525hg17UCSC Ensembl
Outerchr19:22990964..23014157hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3823194
hg1923194
hg1823194
hg1723194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9686
Supporting Variants
SamplesNA10863
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)nssv24120
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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