A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666708



Internal ID9932813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:43935676..43936317hg38UCSC Ensembl
Outerchr20:43935642..43936352hg38UCSC Ensembl
Innerchr20:42564316..42564957hg19UCSC Ensembl
Outerchr20:42564282..42564992hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6576084
SamplesNA20581
Known GenesTOX2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666708
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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