A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3560019



Internal ID18761095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:118895759..118901586hg38UCSC Ensembl
Outerchr2:118895665..118901946hg38UCSC Ensembl
Innerchr2:119653335..119659162hg19UCSC Ensembl
Outerchr2:119653241..119659522hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg386282
hg196282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758766
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3560019
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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