A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9737



Internal ID15500963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:44674838..44703359hg38UCSC Ensembl
Outerchr19:45178110..45206629hg19UCSC Ensembl
Outerchr19:49869950..49898469hg18UCSC Ensembl
Outerchr19:49869950..49898469hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3828522
hg1928520
hg1828520
hg1728520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28561
SamplesNA19221
Known GenesCEACAM16, CEACAM19
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)nsv9737
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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