A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3560738



Internal ID18761814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:191758200..191758232hg38UCSC Ensembl
Outerchr2:191758184..191758249hg38UCSC Ensembl
Innerchr2:192622926..192622958hg19UCSC Ensembl
Outerchr2:192622910..192622975hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9759485
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3560738
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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