A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567168



Internal ID18768244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2568247..2571031hg38UCSC Ensembl
Outerchr6:2567923..2571738hg38UCSC Ensembl
Innerchr6:2568481..2571265hg19UCSC Ensembl
Outerchr6:2568157..2571972hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg383816
hg193816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765915
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567168
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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