A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659914



Internal ID9579333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23765502..23846751hg38UCSC Ensembl
Outerchr20:23765468..23846786hg38UCSC Ensembl
Innerchr20:23746139..23827388hg19UCSC Ensembl
Outerchr20:23746105..23827423hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3881319
hg1981319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv783e199
Supporting Variantsessv6038451
SamplesNA18526
Known GenesCST2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659914
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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