A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25204



Internal ID15492965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31624824..31727381hg38UCSC Ensembl
Outerchr15:31624186..31728450hg38UCSC Ensembl
Innerchr15:31917027..32019584hg19UCSC Ensembl
Outerchr15:31916389..32020653hg19UCSC Ensembl
Innerchr15:29704319..29806876hg18UCSC Ensembl
Outerchr15:29703681..29807945hg18UCSC Ensembl
Innerchr15:29704319..29806876hg17UCSC Ensembl
Outerchr15:29703681..29807945hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38104265
hg19104265
hg18104265
hg17104265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9237
Supporting Variants
SamplesNA18972
Known GenesOTUD7A
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)nssv25204
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer