A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557932



Internal ID18759008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:19551274..19551352hg38UCSC Ensembl
Outerchr22:19551273..19551353hg38UCSC Ensembl
Innerchr22:19538797..19538875hg19UCSC Ensembl
Outerchr22:19538796..19538876hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv282e215
Supporting Variantsessv9756679
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557932
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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