A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893477



Internal ID18837611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33532063..33554551hg38UCSC Ensembl
Outerchr22:33532063..33562703hg38UCSC Ensembl
Innerchr22:33928049..33950537hg19UCSC Ensembl
Outerchr22:33928049..33958689hg19UCSC Ensembl
Innerchr22:32258049..32280537hg18UCSC Ensembl
Outerchr22:32258049..32288689hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3830641
hg1930641
hg1830641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796835, essv25801528
Samples
Known GenesLARGE
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893477
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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