A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8685



Internal ID15846597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:68852817..68868800hg38UCSC Ensembl
Outerchr10:70612573..70628556hg19UCSC Ensembl
Outerchr10:70282579..70298562hg18UCSC Ensembl
Outerchr10:70282579..70298562hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3815984
hg1915984
hg1815984
hg1715984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19010
SamplesNA18853
Known GenesSTOX1
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)nsv8685
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