A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562735



Internal ID18763811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152594030..152595287hg38UCSC Ensembl
Outerchr3:152593878..152595390hg38UCSC Ensembl
Innerchr3:152311819..152313076hg19UCSC Ensembl
Outerchr3:152311667..152313179hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381513
hg191513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761482
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562735
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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