A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6156969



Internal ID9134372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:19541108..19570906hg38UCSC Ensembl
Outerchr22:19541071..19570956hg38UCSC Ensembl
Innerchr22:19528631..19558429hg19UCSC Ensembl
Outerchr22:19528594..19558479hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3829886
hg1929886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659558
Supporting Variants
SamplesNA19066
Known GenesLINC00895
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6156969
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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