A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15041



Internal ID15832073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:374445..375734hg38UCSC Ensembl
Outerchr8:373588..376142hg38UCSC Ensembl
Innerchr8:324445..325734hg19UCSC Ensembl
Outerchr8:323588..326142hg19UCSC Ensembl
Innerchr8:314445..315734hg18UCSC Ensembl
Outerchr8:313588..316142hg18UCSC Ensembl
Innerchr8:314445..315734hg17UCSC Ensembl
Outerchr8:313588..316142hg17UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg382555
hg192555
hg182555
hg172555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8256
Supporting Variants
SamplesNA12872
Known GenesFAM87A
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)nssv15041
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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