A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626939



Internal ID7013769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80860765..80864922hg38UCSC Ensembl
Innerchr11:80860768..80864919hg38UCSC Ensembl
Outerchr11:80860762..80864925hg38UCSC Ensembl
chr11:80571808..80575965hg19UCSC Ensembl
Innerchr11:80571811..80575962hg19UCSC Ensembl
Outerchr11:80571805..80575968hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg384158
hg194158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14216357
SamplesHG01531
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626939
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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