A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656621



Internal ID9922726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25218562..25232074hg38UCSC Ensembl
Outerchr4:25218525..25232124hg38UCSC Ensembl
Innerchr4:25220184..25233696hg19UCSC Ensembl
Outerchr4:25220147..25233746hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3813600
hg1913600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5665219
SamplesNA18636
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656621
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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