A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558136



Internal ID18412526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36852834..36852896hg38UCSC Ensembl
chr22:37248876..37248938hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9756883
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558136
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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