A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27387



Internal ID15496827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32322606..32340517hg38UCSC Ensembl
Outerchr15:32322187..32341072hg38UCSC Ensembl
Innerchr15:32614807..32632718hg19UCSC Ensembl
Outerchr15:32614388..32633273hg19UCSC Ensembl
Innerchr15:30402099..30420010hg18UCSC Ensembl
Outerchr15:30401680..30420565hg18UCSC Ensembl
Innerchr15:30402099..30420010hg17UCSC Ensembl
Outerchr15:30401680..30420565hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3818886
hg1918886
hg1818886
hg1718886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9238
Supporting Variants
SamplesNA19221
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)nssv27387
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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