A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676702



Internal ID9942807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:107159076..107168963hg38UCSC Ensembl
Outerchr5:107159039..107169013hg38UCSC Ensembl
Innerchr5:106494777..106504664hg19UCSC Ensembl
Outerchr5:106494740..106504714hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg389975
hg199975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5445118
SamplesNA18870
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676702
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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