A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14233974



Internal ID5659558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91760374..91764477hg38UCSC Ensembl
Innerchr11:91760374..91764477hg38UCSC Ensembl
Outerchr11:91760187..91764680hg38UCSC Ensembl
chr11:91493540..91497643hg19UCSC Ensembl
Innerchr11:91493540..91497643hg19UCSC Ensembl
Outerchr11:91493353..91497846hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg384104
hg194104
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627260
Supporting Variants
SamplesNA19070
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14233974
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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