A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15665



Internal ID15482217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:72957..170436hg38UCSC Ensembl
Outerchr8:72850..170576hg38UCSC Ensembl
Innerchr8:22957..120436hg19UCSC Ensembl
Outerchr8:22850..120576hg19UCSC Ensembl
Innerchr8:12957..110436hg18UCSC Ensembl
Outerchr8:12850..110576hg18UCSC Ensembl
Innerchr8:12957..110436hg17UCSC Ensembl
Outerchr8:12850..110576hg17UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3897727
hg1997727
hg1897727
hg1797727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8253
Supporting Variants
SamplesNA10847
Known GenesOR4F21
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)nssv15665
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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