A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561378



Internal ID18415768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4047224..4059400hg38UCSC Ensembl
Outerchr3:4046777..4060436hg38UCSC Ensembl
Innerchr3:4088908..4101084hg19UCSC Ensembl
Outerchr3:4088461..4102120hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3813660
hg1913660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760125
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561378
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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