A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26201



Internal ID15832579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101306870..101309503hg38UCSC Ensembl
Outerchr15:101306313..101310486hg38UCSC Ensembl
Innerchr15:101847075..101849708hg19UCSC Ensembl
Outerchr15:101846518..101850691hg19UCSC Ensembl
Innerchr15:99664598..99667231hg18UCSC Ensembl
Outerchr15:99664041..99668214hg18UCSC Ensembl
Innerchr15:99664598..99667231hg17UCSC Ensembl
Outerchr15:99664041..99668214hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg384174
hg194174
hg184174
hg174174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9310
Supporting Variants
SamplesNA18502
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)nssv26201
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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