A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567408



Internal ID18768484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22782444..22782742hg38UCSC Ensembl
Outerchr6:22782376..22782811hg38UCSC Ensembl
Innerchr6:22782673..22782971hg19UCSC Ensembl
Outerchr6:22782605..22783040hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766155
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567408
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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