A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626975



Internal ID7013805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81955689..82048674hg38UCSC Ensembl
Innerchr11:81955689..82048674hg38UCSC Ensembl
Outerchr11:81955189..82049174hg38UCSC Ensembl
chr11:81666731..81759716hg19UCSC Ensembl
Innerchr11:81666731..81759716hg19UCSC Ensembl
Outerchr11:81666231..81760216hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3892986
hg1992986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14218001
SamplesNA12763
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626975
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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