A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678774



Internal ID9944879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24171649..24179948hg38UCSC Ensembl
Outerchr4:24171492..24180101hg38UCSC Ensembl
Innerchr4:24173272..24181571hg19UCSC Ensembl
Outerchr4:24173115..24181724hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg388610
hg198610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5641321
SamplesNA18558
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678774
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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