A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24921



Internal ID15489859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22807212..22807986hg38UCSC Ensembl
Outerchr19:22806652..22808798hg38UCSC Ensembl
Innerchr19:22990014..22990788hg19UCSC Ensembl
Outerchr19:22989454..22991600hg19UCSC Ensembl
Innerchr19:22781854..22782628hg18UCSC Ensembl
Outerchr19:22781294..22783440hg18UCSC Ensembl
Innerchr19:22781854..22782628hg17UCSC Ensembl
Outerchr19:22781294..22783440hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg382147
hg192147
hg182147
hg172147
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9686
Supporting Variants
SamplesNA18564
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)nssv24921
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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