A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22045



Internal ID15840704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24096181..24096522hg38UCSC Ensembl
Outerchr15:24096051..24096965hg38UCSC Ensembl
Innerchr15:24341328..24341669hg19UCSC Ensembl
Outerchr15:24341198..24342112hg19UCSC Ensembl
Innerchr15:21892421..21892762hg18UCSC Ensembl
Outerchr15:21892291..21893205hg18UCSC Ensembl
Innerchr15:21892421..21892762hg17UCSC Ensembl
Outerchr15:21892291..21893205hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38915
hg19915
hg18915
hg17915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA18980
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)nssv22045
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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