A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9228



Internal ID15500454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:29118128..29122991hg38UCSC Ensembl
Outerchr15:29410331..29415194hg19UCSC Ensembl
Outerchr15:27197623..27202486hg18UCSC Ensembl
Outerchr15:27197623..27202486hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg384864
hg194864
hg184864
hg174864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22485
SamplesNA18537
Known GenesAPBA2, FAM189A1
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)nsv9228
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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