A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21506



Internal ID15841139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22022701..22047671hg38UCSC Ensembl
Outerchr15:22018282..22050579hg38UCSC Ensembl
Innerchr15:22310652..22335622hg19UCSC Ensembl
Outerchr15:22306233..22338530hg19UCSC Ensembl
Innerchr15:19812016..19836986hg18UCSC Ensembl
Outerchr15:19807597..19839894hg18UCSC Ensembl
Innerchr15:19812016..19836986hg17UCSC Ensembl
Outerchr15:19807597..19839894hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3832298
hg1932298
hg1832298
hg1732298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA19007
Known GenesLOC727924
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)nssv21506
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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