A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23205



Internal ID15830712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24407593..24512588hg38UCSC Ensembl
Outerchr15:24406490..24519839hg38UCSC Ensembl
Innerchr15:24652740..24757735hg19UCSC Ensembl
Outerchr15:24651637..24764986hg19UCSC Ensembl
Innerchr15:22203833..22308828hg18UCSC Ensembl
Outerchr15:22202730..22316079hg18UCSC Ensembl
Innerchr15:22203833..22308828hg17UCSC Ensembl
Outerchr15:22202730..22316079hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38113350
hg19113350
hg18113350
hg17113350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
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)nssv23205
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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