A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23345



Internal ID15483688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30527283..30536015hg38UCSC Ensembl
Outerchr15:30526810..30536418hg38UCSC Ensembl
Innerchr15:30819486..30828218hg19UCSC Ensembl
Outerchr15:30819013..30828621hg19UCSC Ensembl
Innerchr15:28606778..28615510hg18UCSC Ensembl
Outerchr15:28606305..28615913hg18UCSC Ensembl
Innerchr15:28606778..28615510hg17UCSC Ensembl
Outerchr15:28606305..28615913hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg389609
hg199609
hg189609
hg179609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9232
Supporting Variants
SamplesNA12155
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)nssv23345
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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