A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22977



Internal ID15829810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28286989..28327416hg38UCSC Ensembl
Outerchr15:28281866..28327552hg38UCSC Ensembl
Innerchr15:28532135..28572562hg19UCSC Ensembl
Outerchr15:28527012..28572698hg19UCSC Ensembl
Innerchr15:26205730..26246157hg18UCSC Ensembl
Outerchr15:26200607..26246293hg18UCSC Ensembl
Innerchr15:26205730..26246157hg17UCSC Ensembl
Outerchr15:26200607..26246293hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3845687
hg1945687
hg1845687
hg1745687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9208
Supporting Variants
SamplesNA11830
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)nssv22977
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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