A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8725



Internal ID15499951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:100738036..100743045hg38UCSC Ensembl
Outerchr10:102497793..102502802hg19UCSC Ensembl
Outerchr10:102487783..102492792hg18UCSC Ensembl
Outerchr10:102487783..102492792hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg385010
hg195010
hg185010
hg175010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21702
SamplesNA18502
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)nsv8725
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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