A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5881235



Internal ID9628541
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 StatusS
Merged Variantsesv2674635
Supporting Variants
SamplesNA19350
Known GenesCSNK2A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5881235
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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