A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561857



Internal ID18762933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:49160331..49160580hg38UCSC Ensembl
Outerchr3:49160307..49160645hg38UCSC Ensembl
Innerchr3:49197764..49198013hg19UCSC Ensembl
Outerchr3:49197740..49198078hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760604
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561857
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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