A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665557



Internal ID9931662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86416941..86418093hg38UCSC Ensembl
chr3:86466091..86467243hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg381153
hg191153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5448561
SamplesNA18617
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665557
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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