A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22919



Internal ID15829815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24126323..24137667hg38UCSC Ensembl
Outerchr15:24125241..24139111hg38UCSC Ensembl
Innerchr15:24371470..24382814hg19UCSC Ensembl
Outerchr15:24370388..24384258hg19UCSC Ensembl
Innerchr15:21922563..21933907hg18UCSC Ensembl
Outerchr15:21921481..21935351hg18UCSC Ensembl
Innerchr15:21922563..21933907hg17UCSC Ensembl
Outerchr15:21921481..21935351hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3813871
hg1913871
hg1813871
hg1713871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA11830
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)nssv22919
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