A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756428



Internal ID18730674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36303821..36304016hg38UCSC Ensembl
Outerchr21:36303769..36304083hg38UCSC Ensembl
Innerchr21:37676119..37676314hg19UCSC Ensembl
Outerchr21:37676067..37676381hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557681
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756428
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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