A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656963



Internal ID9576382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22389282..22391864hg38UCSC Ensembl
Outerchr4:22389125..22392022hg38UCSC Ensembl
Innerchr4:22390905..22393487hg19UCSC Ensembl
Outerchr4:22390748..22393645hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382898
hg192898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5677002
SamplesHG00259
Known GenesGPR125
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656963
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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