A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22949



Internal ID15830813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21192131..21193253hg38UCSC Ensembl
Innerchr15:21397460..21398582hg19UCSC Ensembl
Innerchr15:19662119..19663241hg18UCSC Ensembl
Innerchr15:19662119..19663241hg17UCSC Ensembl
Outerchr15:19661464..19763507hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381123
hg191123
hg181123
hg17102044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12155
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)nssv22949
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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