A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22449



Internal ID15831107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21174031..21176692hg38UCSC Ensembl
Outerchr15:21173569..21177375hg38UCSC Ensembl
Innerchr15:21379360..21382021hg19UCSC Ensembl
Outerchr15:21378898..21382704hg19UCSC Ensembl
Innerchr15:19644019..19646680hg18UCSC Ensembl
Outerchr15:19643557..19647363hg18UCSC Ensembl
Innerchr15:19644019..19646680hg17UCSC Ensembl
Outerchr15:19643557..19647363hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg383807
hg193807
hg183807
hg173807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12740
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)nssv22449
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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