A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9664



Internal ID15500890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:8208439..8210323hg38UCSC Ensembl
Outerchr19:8273323..8275207hg19UCSC Ensembl
Outerchr19:8179323..8181207hg18UCSC Ensembl
Outerchr19:8179323..8181207hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381885
hg191885
hg181885
hg171885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27255
SamplesNA19132
Known GenesCERS4
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)nsv9664
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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