A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22075



Internal ID15840695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24265807..24294142hg38UCSC Ensembl
Outerchr15:24261163..24295310hg38UCSC Ensembl
Innerchr15:24510954..24539289hg19UCSC Ensembl
Outerchr15:24506310..24540457hg19UCSC Ensembl
Innerchr15:22062047..22090382hg18UCSC Ensembl
Outerchr15:22057403..22091550hg18UCSC Ensembl
Innerchr15:22062047..22090382hg17UCSC Ensembl
Outerchr15:22057403..22091550hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3834148
hg1934148
hg1834148
hg1734148
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)nssv22075
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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