A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756806



Internal ID18731052
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 StatusS
Merged Variantsesv3558059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756806
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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