A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21510



Internal ID15843796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85939688..85942416hg38UCSC Ensembl
Outerchr8:85939018..85943587hg38UCSC Ensembl
Innerchr8:86951917..86954645hg19UCSC Ensembl
Outerchr8:86951247..86955816hg19UCSC Ensembl
Innerchr8:87021033..87023761hg18UCSC Ensembl
Outerchr8:87020363..87024932hg18UCSC Ensembl
Innerchr8:87021033..87023761hg17UCSC Ensembl
Outerchr8:87020363..87024932hg17UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg384570
hg194570
hg184570
hg174570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8363
Supporting Variants
SamplesNA19221
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)nssv21510
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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