A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562531



Internal ID18763607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129639216..129640322hg38UCSC Ensembl
Outerchr3:129638979..129640342hg38UCSC Ensembl
Innerchr3:129358059..129359165hg19UCSC Ensembl
Outerchr3:129357822..129359185hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761278
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562531
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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