A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675861



Internal ID9941966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133053728..133090685hg38UCSC Ensembl
Outerchr4:133053691..133090735hg38UCSC Ensembl
Innerchr4:133974883..134011840hg19UCSC Ensembl
Outerchr4:133974846..134011890hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3837045
hg1937045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5866075
SamplesHG00335
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675861
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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