A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6379093



Internal ID9803468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:27014329..27019327hg38UCSC Ensembl
Outerchr22:27014292..27019377hg38UCSC Ensembl
Innerchr22:27410292..27415290hg19UCSC Ensembl
Outerchr22:27410255..27415340hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg385086
hg195086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666282
Supporting Variants
SamplesNA19901
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6379093
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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