A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22920



Internal ID15830809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21051813..21057922hg38UCSC Ensembl
Outerchr15:21051231..21058249hg38UCSC Ensembl
Innerchr15:21257142..21263251hg19UCSC Ensembl
Outerchr15:21256560..21263578hg19UCSC Ensembl
Innerchr15:19521801..19527910hg18UCSC Ensembl
Outerchr15:19521219..19528237hg18UCSC Ensembl
Innerchr15:19521801..19527910hg17UCSC Ensembl
Outerchr15:19521219..19528237hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387019
hg197019
hg187019
hg177019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12155
Known Genes
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)nssv22920
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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