A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563563



Internal ID18764639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24501488..24502490hg38UCSC Ensembl
Outerchr4:24501247..24502646hg38UCSC Ensembl
Innerchr4:24503111..24504113hg19UCSC Ensembl
Outerchr4:24502870..24504269hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762310
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563563
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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