A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22499



Internal ID15843090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28249982..28255700hg38UCSC Ensembl
Outerchr15:28249406..28256496hg38UCSC Ensembl
Innerchr15:28495128..28500846hg19UCSC Ensembl
Outerchr15:28494552..28501642hg19UCSC Ensembl
Innerchr15:26168723..26174441hg18UCSC Ensembl
Outerchr15:26168147..26175237hg18UCSC Ensembl
Innerchr15:26168723..26174441hg17UCSC Ensembl
Outerchr15:26168147..26175237hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg387091
hg197091
hg187091
hg177091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9206
Supporting Variants
SamplesNA19173
Known GenesHERC2
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)nssv22499
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