A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627975



Internal ID6668119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124318013..124328419hg38UCSC Ensembl
Innerchr11:124318163..124328269hg38UCSC Ensembl
Outerchr11:124317863..124328569hg38UCSC Ensembl
chr11:124187909..124198315hg19UCSC Ensembl
Innerchr11:124188059..124198165hg19UCSC Ensembl
Outerchr11:124187759..124198465hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3810407
hg1910407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14301923
SamplesHG02057
Known GenesOR8D2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627975
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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