A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610538



Internal ID16051261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15544498..15554587hg38UCSC Ensembl
Innerchr8:15402007..15412096hg19UCSC Ensembl
Innerchr8:15446378..15456467hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3810090
hg1910090
hg1810090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12014n54
Supporting Variantsnssv1106891, nssv1106881, nssv1106897, nssv1106895, nssv1106885, nssv1106893, nssv1106886, nssv1106892, nssv1106890, nssv1106894, nssv1106887, nssv1106883, nssv1106896, nssv1106884, nssv1106882, nssv1106879, nssv1106889, nssv1106888, nssv1106880, nssv1106898
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610538
Frequency
Sample Size17421
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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