A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627355



Internal ID7014185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95540524..95552110hg38UCSC Ensembl
Innerchr11:95540533..95552101hg38UCSC Ensembl
Outerchr11:95540515..95552119hg38UCSC Ensembl
chr11:95273688..95285274hg19UCSC Ensembl
Innerchr11:95273697..95285265hg19UCSC Ensembl
Outerchr11:95273679..95285283hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3811587
hg1911587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14243589
SamplesNA19717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627355
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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