A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25506



Internal ID15838415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20808886..20810637hg38UCSC Ensembl
Outerchr15:20808236..20813553hg38UCSC Ensembl
Innerchr15:21014215..21015966hg19UCSC Ensembl
Outerchr15:21013565..21018882hg19UCSC Ensembl
Innerchr15:19274256..19276015hg18UCSC Ensembl
Outerchr15:19273606..19278933hg18UCSC Ensembl
Innerchr15:19274256..19276015hg17UCSC Ensembl
Outerchr15:19273606..19278933hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg385318
hg195318
hg185328
hg175328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18860
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)nssv25506
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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