A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9217



Internal ID15847129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:28656380..28665794hg38UCSC Ensembl
Outerchr15:28901526..28910940hg19UCSC Ensembl
Outerchr15:26700567..26709981hg18UCSC Ensembl
Outerchr15:26700567..26709981hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg389415
hg199415
hg189415
hg179415
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24432, nssv23120, nssv21826
SamplesNA11830, NA19240, NA18552
Known GenesHERC2P9
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)nsv9217
Frequency
Sample Size31
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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