A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9668



Internal ID15500894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15101800..15131511hg38UCSC Ensembl
Outerchr19:15212611..15242322hg19UCSC Ensembl
Outerchr19:15073611..15103322hg18UCSC Ensembl
Outerchr19:15073611..15103322hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3829712
hg1929712
hg1829712
hg1729712
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28454, nssv27438
SamplesNA18502, NA19221
Known GenesILVBL, SYDE1
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)nsv9668
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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