A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19480



Internal ID15831891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24136081..24153762hg38UCSC Ensembl
Outerchr15:24133143..24158041hg38UCSC Ensembl
Innerchr15:24381228..24398909hg19UCSC Ensembl
Outerchr15:24378290..24403188hg19UCSC Ensembl
Innerchr15:21932321..21950002hg18UCSC Ensembl
Outerchr15:21929383..21954281hg18UCSC Ensembl
Innerchr15:21932321..21950002hg17UCSC Ensembl
Outerchr15:21929383..21954281hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3824899
hg1924899
hg1824899
hg1724899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA12802
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)nssv19480
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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