A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626758



Internal ID6666906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69969671..69976259hg38UCSC Ensembl
Innerchr11:69969671..69976259hg38UCSC Ensembl
Outerchr11:69969441..69976523hg38UCSC Ensembl
chr11:69815777..69822365hg19UCSC Ensembl
Innerchr11:69815777..69822365hg19UCSC Ensembl
Outerchr11:69815547..69822629hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg386589
hg196589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14207083, essv14207084
SamplesHG01440, HG01124
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626758
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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