A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6255145



Internal ID8753229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56831195..56853219hg38UCSC Ensembl
Outerchr20:56831158..56853269hg38UCSC Ensembl
Innerchr20:55406251..55428275hg19UCSC Ensembl
Outerchr20:55406214..55428325hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3822112
hg1922112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667179
Supporting Variants
SamplesHG00142
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6255145
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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