A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557606



Internal ID18758682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:28862429..28862614hg38UCSC Ensembl
Outerchr21:28862345..28862703hg38UCSC Ensembl
Innerchr21:30234751..30234936hg19UCSC Ensembl
Outerchr21:30234667..30235025hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9756353
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557606
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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