A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756450



Internal ID18384010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38528465..38528741hg38UCSC Ensembl
Outerchr21:38528392..38528792hg38UCSC Ensembl
Innerchr21:39900389..39900665hg19UCSC Ensembl
Outerchr21:39900316..39900716hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557703
Supporting Variants
Samples
Known GenesERG
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756450
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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