A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668268



Internal ID9934373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:75904697..75910571hg38UCSC Ensembl
Outerchr4:75904660..75910621hg38UCSC Ensembl
Innerchr4:76825850..76831724hg19UCSC Ensembl
Outerchr4:76825813..76831774hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg385962
hg195962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5655075
SamplesNA18940
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668268
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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