A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660434



Internal ID9579853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:35633935..35634526hg38UCSC Ensembl
Outerchr20:35633898..35634576hg38UCSC Ensembl
Innerchr20:34221857..34222448hg19UCSC Ensembl
Outerchr20:34221820..34222498hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6518702, essv6498171, essv5446657
SamplesNA19093, NA18516, NA19452
Known GenesCPNE1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660434
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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