A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557699



Internal ID18758775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38218619..38218948hg38UCSC Ensembl
Outerchr21:38218544..38218978hg38UCSC Ensembl
Innerchr21:39590541..39590870hg19UCSC Ensembl
Outerchr21:39590466..39590900hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9756446
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557699
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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