A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760563



Internal ID18388123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:45568425..45568738hg38UCSC Ensembl
Outerchr3:45568327..45568811hg38UCSC Ensembl
Innerchr3:45609917..45610230hg19UCSC Ensembl
Outerchr3:45609819..45610303hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760563
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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