A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677051



Internal ID9943156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:140323896..140324238hg38UCSC Ensembl
Outerchr5:140323859..140324288hg38UCSC Ensembl
Innerchr5:139703481..139703823hg19UCSC Ensembl
Outerchr5:139703444..139703873hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5805403
SamplesNA19190
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677051
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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