A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561798



Internal ID18416188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:42989614..42989884hg38UCSC Ensembl
Outerchr3:42989556..42989959hg38UCSC Ensembl
Innerchr3:43031106..43031376hg19UCSC Ensembl
Outerchr3:43031048..43031451hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760545
Samples
Known GenesFAM198A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561798
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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