A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675016



Internal ID9941121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26462398..26465982hg38UCSC Ensembl
Outerchr3:26462241..26466135hg38UCSC Ensembl
Innerchr3:26503889..26507473hg19UCSC Ensembl
Outerchr3:26503732..26507626hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg383895
hg193895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6049295
SamplesHG00404
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675016
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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