A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558131



Internal ID18759207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36731029..36731200hg38UCSC Ensembl
Outerchr22:36730993..36731233hg38UCSC Ensembl
Innerchr22:37127074..37127245hg19UCSC Ensembl
Outerchr22:37127038..37127278hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9756878
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558131
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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