A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558059



Internal ID18759135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:31051595..31052453hg38UCSC Ensembl
Outerchr22:31051510..31052580hg38UCSC Ensembl
Innerchr22:31447581..31448439hg19UCSC Ensembl
Outerchr22:31447496..31448566hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381071
hg191071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9756806
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558059
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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