A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25621



Internal ID15838177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22012852..22014082hg38UCSC Ensembl
Outerchr15:22012461..22014536hg38UCSC Ensembl
Innerchr15:22300803..22302033hg19UCSC Ensembl
Outerchr15:22300412..22302487hg19UCSC Ensembl
Innerchr15:19802167..19803397hg18UCSC Ensembl
Outerchr15:19801776..19803851hg18UCSC Ensembl
Innerchr15:19802167..19803397hg17UCSC Ensembl
Outerchr15:19801776..19803851hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382076
hg192076
hg182076
hg172076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18860
Known GenesLOC727924
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)nssv25621
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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