A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756908



Internal ID18384468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38666192..38666262hg38UCSC Ensembl
chr22:39062197..39062267hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558161
Supporting Variants
Samples
Known GenesCBY1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756908
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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