A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14286901



Internal ID5115451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111344515..111347763hg38UCSC Ensembl
chr11:111215240..111218488hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg383249
hg193249
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627736
Supporting Variants
SamplesNA18560
Known GenesMIR4491
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14286901
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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