A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562107



Internal ID18416497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77292365..77293009hg38UCSC Ensembl
Outerchr3:77292266..77293090hg38UCSC Ensembl
Innerchr3:77341516..77342160hg19UCSC Ensembl
Outerchr3:77341417..77342241hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38825
hg19825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760854
Samples
Known GenesROBO2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562107
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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