A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627743



Internal ID6667890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111769259..111771708hg38UCSC Ensembl
Innerchr11:111769259..111771708hg38UCSC Ensembl
Outerchr11:111769037..111771900hg38UCSC Ensembl
chr11:111639983..111642432hg19UCSC Ensembl
Innerchr11:111639983..111642432hg19UCSC Ensembl
Outerchr11:111639761..111642624hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg382450
hg192450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14287032
SamplesHG01461
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627743
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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