A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567465



Internal ID18768541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:28050415..28054076hg38UCSC Ensembl
Outerchr6:28050408..28054110hg38UCSC Ensembl
Innerchr6:28018193..28021854hg19UCSC Ensembl
Outerchr6:28018186..28021888hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg383703
hg193703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766212
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567465
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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