A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674191



Internal ID9940296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3308392..3311219hg38UCSC Ensembl
chr17:3211686..3214513hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg382828
hg192828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5996946
SamplesNA19713
Known GenesOR3A4P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674191
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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