A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8686



Internal ID15846598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:69512188..69516116hg38UCSC Ensembl
Outerchr10:71271944..71275872hg19UCSC Ensembl
Outerchr10:70941950..70945878hg18UCSC Ensembl
Outerchr10:70941950..70945878hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383929
hg193929
hg183929
hg173929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24327
SamplesNA19221
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)nsv8686
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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