A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674635



Internal ID9940740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:523827..525565hg38UCSC Ensembl
Outerchr20:523757..525639hg38UCSC Ensembl
Innerchr20:504471..506209hg19UCSC Ensembl
Outerchr20:504401..506283hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381883
hg191883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5881235, essv6111608, essv5569873
SamplesNA19397, NA19350, NA19396
Known GenesCSNK2A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674635
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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