A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612303



Internal ID16399712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:130839180..130840053hg38UCSC Ensembl
Innerchr8:131851426..131852299hg19UCSC Ensembl
Innerchr8:131920608..131921481hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38874
hg19874
hg18874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12335n54
Supporting Variantsnssv1121497
Samples
Known GenesADCY8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612303
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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