A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612954



Internal ID16053677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144493267..144495299hg38UCSC Ensembl
Innerchr8:145718650..145720682hg19UCSC Ensembl
Innerchr8:145689458..145691490hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg382033
hg192033
hg182033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12441n54
Supporting Variantsnssv1125816
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612954
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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