A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22256



Internal ID15494377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30528938..30541559hg38UCSC Ensembl
Outerchr15:30528347..30542169hg38UCSC Ensembl
Innerchr15:30821141..30833762hg19UCSC Ensembl
Outerchr15:30820550..30834372hg19UCSC Ensembl
Innerchr15:28608433..28621054hg18UCSC Ensembl
Outerchr15:28607842..28621664hg18UCSC Ensembl
Innerchr15:28608433..28621054hg17UCSC Ensembl
Outerchr15:28607842..28621664hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3813823
hg1913823
hg1813823
hg1713823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9232
Supporting Variants
SamplesNA19007
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)nssv22256
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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