A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661867



Internal ID9927972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65455485..65468712hg38UCSC Ensembl
chr3:65441160..65454387hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3813228
hg1913228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6283403
SamplesNA12342
Known GenesMAGI1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661867
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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