A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763549



Internal ID18737795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:151970304..151972109hg38UCSC Ensembl
Outerchr4:151970261..151972566hg38UCSC Ensembl
Innerchr4:152891456..152893261hg19UCSC Ensembl
Outerchr4:152891413..152893718hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382306
hg192306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564802
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763549
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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