A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567468



Internal ID18768544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:28222443..28222731hg38UCSC Ensembl
Outerchr6:28222375..28222824hg38UCSC Ensembl
Innerchr6:28190221..28190509hg19UCSC Ensembl
Outerchr6:28190153..28190602hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766215
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567468
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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