A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666798



Internal ID9932903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:56852336..56862124hg38UCSC Ensembl
Outerchr3:56852299..56862174hg38UCSC Ensembl
Innerchr3:56886364..56896152hg19UCSC Ensembl
Outerchr3:56886327..56896202hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg389876
hg199876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5699129
SamplesHG00237
Known GenesARHGEF3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666798
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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