A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562500



Internal ID18763576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:125953658..125957261hg38UCSC Ensembl
Outerchr3:125953233..125958157hg38UCSC Ensembl
Innerchr3:125672501..125676104hg19UCSC Ensembl
Outerchr3:125672076..125677000hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg384925
hg194925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761247
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562500
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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