A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19377



Internal ID15495481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15800820..15801554hg38UCSC Ensembl
Outerchr8:15795556..15802199hg38UCSC Ensembl
Innerchr8:15658329..15659063hg19UCSC Ensembl
Outerchr8:15653065..15659708hg19UCSC Ensembl
Innerchr8:15702700..15703434hg18UCSC Ensembl
Outerchr8:15697436..15704079hg18UCSC Ensembl
Innerchr8:15702700..15703434hg17UCSC Ensembl
Outerchr8:15697436..15704079hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg386644
hg196644
hg186644
hg176644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8298
Supporting Variants
SamplesNA19132
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)nssv19377
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