A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8599



Internal ID15499825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5607166..5677965hg38UCSC Ensembl
Outerchr10:5649129..5719928hg19UCSC Ensembl
Outerchr10:5689135..5759934hg18UCSC Ensembl
Outerchr10:5689135..5759934hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3870800
hg1970800
hg1870800
hg1770800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21567
SamplesNA19132
Known GenesASB13
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)nsv8599
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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