A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14285863



Internal ID632953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110501121..110502533hg38UCSC Ensembl
Innerchr11:110501169..110502486hg38UCSC Ensembl
Outerchr11:110501074..110502581hg38UCSC Ensembl
chr11:110371845..110373257hg19UCSC Ensembl
Innerchr11:110371893..110373210hg19UCSC Ensembl
Outerchr11:110371798..110373305hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381413
hg191413
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627720
Supporting Variants
SamplesHG00276
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14285863
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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