A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662528



Internal ID9928633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2039338..2066091hg38UCSC Ensembl
Outerchr5:2039301..2066141hg38UCSC Ensembl
Innerchr5:2039452..2066205hg19UCSC Ensembl
Outerchr5:2039415..2066255hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3826841
hg1926841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5771892
SamplesNA20585
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662528
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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