A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626944



Internal ID7013774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81127227..81128322hg38UCSC Ensembl
Innerchr11:81127248..81128302hg38UCSC Ensembl
Outerchr11:81127207..81128343hg38UCSC Ensembl
chr11:80838270..80839365hg19UCSC Ensembl
Innerchr11:80838291..80839345hg19UCSC Ensembl
Outerchr11:80838250..80839386hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14216398, essv14216401, essv14216400, essv14216402, essv14216399
SamplesHG00233, HG02687, NA11918, NA20536, HG03634
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626944
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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