A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24272



Internal ID15844799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28204172..28239662hg38UCSC Ensembl
Outerchr15:28203819..28240506hg38UCSC Ensembl
Innerchr15:28449318..28484808hg19UCSC Ensembl
Outerchr15:28448965..28485652hg19UCSC Ensembl
Innerchr15:26122913..26158403hg18UCSC Ensembl
Outerchr15:26122560..26159247hg18UCSC Ensembl
Innerchr15:26122913..26158403hg17UCSC Ensembl
Outerchr15:26122560..26159247hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3836688
hg1936688
hg1836688
hg1736688
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9205
Supporting Variants
SamplesNA19240
Known GenesHERC2
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)nssv24272
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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