A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627531



Internal ID7014359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102543597..102554596hg38UCSC Ensembl
Innerchr11:102543611..102554582hg38UCSC Ensembl
Outerchr11:102543583..102554610hg38UCSC Ensembl
chr11:102414328..102425327hg19UCSC Ensembl
Innerchr11:102414342..102425313hg19UCSC Ensembl
Outerchr11:102414314..102425341hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3811000
hg1911000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14254818
SamplesNA18951
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627531
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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