A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664121



Internal ID9930226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3495472..3505340hg38UCSC Ensembl
Outerchr20:3495435..3505390hg38UCSC Ensembl
Innerchr20:3476119..3485987hg19UCSC Ensembl
Outerchr20:3476082..3486037hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg389956
hg199956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6466892
SamplesNA19449
Known GenesATRN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664121
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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