A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562589



Internal ID18416979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:134955157..134955692hg38UCSC Ensembl
Outerchr3:134955027..134955746hg38UCSC Ensembl
Innerchr3:134673999..134674534hg19UCSC Ensembl
Outerchr3:134673869..134674588hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761336
Samples
Known GenesEPHB1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562589
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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