A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664205



Internal ID9583624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5409720..5471177hg38UCSC Ensembl
Outerchr11:5409683..5471227hg38UCSC Ensembl
Innerchr11:5430950..5492407hg19UCSC Ensembl
Outerchr11:5430913..5492457hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3861545
hg1961545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6119028
SamplesNA19066
Known GenesOR51B5, OR51I1, OR51I2, OR51Q1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664205
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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