A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3539855



Internal ID18740971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:63957189..63958374hg38UCSC Ensembl
Outerchr6:63957064..63958577hg38UCSC Ensembl
Innerchr6:64667082..64668267hg19UCSC Ensembl
Outerchr6:64666957..64668470hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381514
hg191514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9738602
Samples
Known GenesEYS
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3539855
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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