A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611608



Internal ID16052331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:81464464..81480614hg38UCSC Ensembl
Innerchr8:82376699..82392849hg19UCSC Ensembl
Innerchr8:82539254..82555404hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3816151
hg1916151
hg1816151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117306
Samples
Known GenesFABP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611608
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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