A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25345



Internal ID15832966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23174518..23182103hg38UCSC Ensembl
Outerchr15:23174492..23182538hg38UCSC Ensembl
Innerchr15:22690965..22698550hg19UCSC Ensembl
Outerchr15:22690530..22698899hg19UCSC Ensembl
Innerchr15:20242329..20249914hg18UCSC Ensembl
Outerchr15:20241894..20250263hg18UCSC Ensembl
Innerchr15:20242329..20249914hg17UCSC Ensembl
Outerchr15:20241894..20250263hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg388047
hg198370
hg188370
hg178370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9181
Supporting Variants
SamplesNA18502
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)nssv25345
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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