A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25475



Internal ID15833143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24080111..24099953hg38UCSC Ensembl
Outerchr15:24079653..24100295hg38UCSC Ensembl
Innerchr15:24325258..24345100hg19UCSC Ensembl
Outerchr15:24324800..24345442hg19UCSC Ensembl
Innerchr15:21876351..21896193hg18UCSC Ensembl
Outerchr15:21875893..21896535hg18UCSC Ensembl
Innerchr15:21876351..21896193hg17UCSC Ensembl
Outerchr15:21875893..21896535hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3820643
hg1920643
hg1820643
hg1720643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA18502
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)nssv25475
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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