A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23822



Internal ID15830821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101306870..101308607hg38UCSC Ensembl
Outerchr15:101306313..101309503hg38UCSC Ensembl
Innerchr15:101847075..101848812hg19UCSC Ensembl
Outerchr15:101846518..101849708hg19UCSC Ensembl
Innerchr15:99664598..99666335hg18UCSC Ensembl
Outerchr15:99664041..99667231hg18UCSC Ensembl
Innerchr15:99664598..99666335hg17UCSC Ensembl
Outerchr15:99664041..99667231hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg383191
hg193191
hg183191
hg173191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9310
Supporting Variants
SamplesNA12155
Known GenesLOC100507472, PCSK6
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)nssv23822
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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