A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15341



Internal ID15485426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7516704..7516957hg38UCSC Ensembl
Outerchr8:7516374..7517135hg38UCSC Ensembl
Innerchr8:7374226..7374479hg19UCSC Ensembl
Outerchr8:7373896..7374657hg19UCSC Ensembl
Innerchr8:7361636..7361889hg18UCSC Ensembl
Outerchr8:7361306..7362067hg18UCSC Ensembl
Innerchr8:7361636..7361889hg17UCSC Ensembl
Outerchr8:7361306..7362067hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38762
hg19762
hg18762
hg17762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8281
Supporting Variants
SamplesNA12872
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)nssv15341
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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