A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612086



Internal ID16399495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119143775..119156302hg38UCSC Ensembl
Innerchr8:120156014..120168541hg19UCSC Ensembl
Innerchr8:120225195..120237722hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3812528
hg1912528
hg1812528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12298n54
Supporting Variantsnssv1120386
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612086
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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