A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627713



Internal ID6667860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109886535..109887683hg38UCSC Ensembl
Innerchr11:109886538..109887681hg38UCSC Ensembl
Outerchr11:109886533..109887686hg38UCSC Ensembl
chr11:109757261..109758409hg19UCSC Ensembl
Innerchr11:109757264..109758407hg19UCSC Ensembl
Outerchr11:109757259..109758412hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381149
hg191149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14280583, essv14280582
SamplesHG01840, HG01862
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627713
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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