A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25604



Internal ID15496554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15667434..15671007hg38UCSC Ensembl
Outerchr19:15666486..15671803hg38UCSC Ensembl
Innerchr19:15778244..15781817hg19UCSC Ensembl
Outerchr19:15777296..15782613hg19UCSC Ensembl
Innerchr19:15639244..15642817hg18UCSC Ensembl
Outerchr19:15638296..15643613hg18UCSC Ensembl
Innerchr19:15639244..15642817hg17UCSC Ensembl
Outerchr19:15638296..15643613hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg385318
hg195318
hg185318
hg175318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9671
Supporting Variants
SamplesNA19173
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)nssv25604
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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