A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24098



Internal ID15833494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23190651..23194729hg38UCSC Ensembl
Outerchr15:23189557..23197946hg38UCSC Ensembl
Innerchr15:22678339..22682417hg19UCSC Ensembl
Outerchr15:22675122..22683511hg19UCSC Ensembl
Innerchr15:20229703..20233781hg18UCSC Ensembl
Outerchr15:20226486..20234875hg18UCSC Ensembl
Innerchr15:20229703..20233781hg17UCSC Ensembl
Outerchr15:20226486..20234875hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg388390
hg198390
hg188390
hg178390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9181
Supporting Variants
SamplesNA18504
Known GenesMIR4509-1, MIR4509-2, MIR4509-3
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)nssv24098
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