A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559592



Internal ID18760668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139511733..139511783hg38UCSC Ensembl
chr3:139230575..139230625hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv304e215
Supporting Variantsessv9758339
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559592
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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