A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890865



Internal ID18838481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64517204..65033535hg38UCSC Ensembl
Outerchr6:64517204..65033535hg38UCSC Ensembl
Innerchr6:65227097..65743428hg19UCSC Ensembl
Outerchr6:65227097..65743428hg19UCSC Ensembl
Innerchr6:65283818..65800149hg18UCSC Ensembl
Outerchr6:65283818..65800149hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38516332
hg19516332
hg18516332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781598
Samples
Known GenesEYS
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890865
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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