A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22504



Internal ID15828386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101904359..101904359hg38UCSC Ensembl
Outerchr15:101897454..101904476hg38UCSC Ensembl
Innerchr15:102444562..102444562hg19UCSC Ensembl
Outerchr15:102437657..102444679hg19UCSC Ensembl
Innerchr15:100262085..100262085hg18UCSC Ensembl
Outerchr15:100255180..100262202hg18UCSC Ensembl
Innerchr15:100262085..100262085hg17UCSC Ensembl
Outerchr15:100255180..100262202hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg387023
hg197023
hg187023
hg177023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9315
Supporting Variants
SamplesNA10839
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)nssv22504
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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