A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561707



Internal ID18762783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32765353..32766342hg38UCSC Ensembl
Outerchr3:32765229..32766611hg38UCSC Ensembl
Innerchr3:32806845..32807834hg19UCSC Ensembl
Outerchr3:32806721..32808103hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381383
hg191383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760454
Samples
Known GenesCNOT10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561707
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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