A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677437



Internal ID9596856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:43405810..43414080hg38UCSC Ensembl
Outerchr5:43405773..43414130hg38UCSC Ensembl
Innerchr5:43405912..43414182hg19UCSC Ensembl
Outerchr5:43405875..43414232hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg388358
hg198358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5981733
SamplesHG00536
Known GenesCCL28
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677437
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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