A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625855



Internal ID7012689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32206045..32207573hg38UCSC Ensembl
Innerchr11:32206058..32207561hg38UCSC Ensembl
Outerchr11:32206033..32207586hg38UCSC Ensembl
chr11:32227591..32229119hg19UCSC Ensembl
Innerchr11:32227604..32229107hg19UCSC Ensembl
Outerchr11:32227579..32229132hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381529
hg191529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14080050, essv14080051
SamplesHG01802, HG02391
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625855
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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