A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9227



Internal ID15500453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:29053409..29055623hg38UCSC Ensembl
Outerchr15:29345612..29347826hg19UCSC Ensembl
Outerchr15:27132904..27135118hg18UCSC Ensembl
Outerchr15:27132904..27135118hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382215
hg192215
hg182215
hg172215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23261, nssv22046, nssv23176, nssv24458, nssv27237, nssv22264, nssv22128, nssv26063
SamplesNA10839, NA18860, NA12155, NA18564, NA19221, NA11830, NA19240, NA19007
Known GenesAPBA2
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)nsv9227
Frequency
Sample Size31
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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