A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669598



Internal ID9935703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143106361..143127733hg38UCSC Ensembl
Outerchr8:143106204..143127886hg38UCSC Ensembl
Innerchr8:144187778..144209150hg19UCSC Ensembl
Outerchr8:144187621..144209303hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3821683
hg1921683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5891490
SamplesHG01124
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669598
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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