A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8739



Internal ID15846651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:126084024..126087972hg38UCSC Ensembl
Outerchr10:127772593..127776541hg19UCSC Ensembl
Outerchr10:127762583..127766531hg18UCSC Ensembl
Outerchr10:127762583..127766531hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg383949
hg193949
hg183949
hg173949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19340
SamplesNA18853
Known GenesADAM12
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)nsv8739
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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