A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657209



Internal ID9923314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:155745538..155746573hg38UCSC Ensembl
Outerchr5:155745501..155746623hg38UCSC Ensembl
Innerchr5:155125098..155126133hg19UCSC Ensembl
Outerchr5:155125061..155126183hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg381123
hg191123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6510325
SamplesHG00342
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657209
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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