A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14278429



Internal ID4001530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108802210..108823070hg38UCSC Ensembl
Innerchr11:108802710..108822570hg38UCSC Ensembl
Outerchr11:108801210..108824070hg38UCSC Ensembl
chr11:108672937..108693797hg19UCSC Ensembl
Innerchr11:108673437..108693297hg19UCSC Ensembl
Outerchr11:108671937..108694797hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3820861
hg1920861
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627685
Supporting Variants
SamplesHG03652
Known GenesDDX10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14278429
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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