A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9620



Internal ID15847532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:14868405..14896941hg38UCSC Ensembl
Outerchr18:14868404..14896940hg19UCSC Ensembl
Outerchr18:14858404..14886940hg18UCSC Ensembl
Outerchr18:14858404..14886940hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3828537
hg1928537
hg1828537
hg1728537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27300, nssv24207
SamplesNA18502, NA18563
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)nsv9620
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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