A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657647



Internal ID9577066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61881802..61885475hg38UCSC Ensembl
Outerchr11:61881645..61885628hg38UCSC Ensembl
Innerchr11:61649274..61652947hg19UCSC Ensembl
Outerchr11:61649117..61653100hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg383984
hg193984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv217e199
Supporting Variantsessv6094730
SamplesNA19471
Known GenesFADS3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657647
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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