A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756438



Internal ID18730684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:37589434..37589675hg38UCSC Ensembl
Outerchr21:37589352..37589730hg38UCSC Ensembl
Innerchr21:38961736..38961977hg19UCSC Ensembl
Outerchr21:38961654..38962032hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557691
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756438
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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