A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658298



Internal ID9924403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6168511..6171691hg38UCSC Ensembl
Outerchr11:6168354..6171844hg38UCSC Ensembl
Innerchr11:6189741..6192921hg19UCSC Ensembl
Outerchr11:6189584..6193074hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383491
hg193491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6492970, essv5856051, essv5767334, essv6504490, essv6546964
SamplesNA18504, NA18489, NA19239, NA19147, NA19129
Known GenesOR52B2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658298
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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