A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15829



Internal ID15490309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7714883..7774492hg38UCSC Ensembl
Outerchr8:7713521..7774564hg38UCSC Ensembl
Innerchr8:7572405..7632014hg19UCSC Ensembl
Outerchr8:7571043..7632086hg19UCSC Ensembl
Innerchr8:7609815..7669424hg18UCSC Ensembl
Outerchr8:7608453..7669496hg18UCSC Ensembl
Innerchr8:7609815..7669424hg17UCSC Ensembl
Outerchr8:7608453..7669496hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3861044
hg1961044
hg1861044
hg1761044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8281
Supporting Variants
SamplesNA18572
Known GenesFAM90A10P
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)nssv15829
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