A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557895



Internal ID18758971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17290364..17297608hg38UCSC Ensembl
Outerchr22:17289301..17298304hg38UCSC Ensembl
Innerchr22:17771254..17778498hg19UCSC Ensembl
Outerchr22:17770191..17779194hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg389004
hg199004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9756642
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557895
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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