A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14302966



Internal ID2855157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126365411..126381998hg38UCSC Ensembl
chr11:126235306..126251893hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3816588
hg1916588
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628004
Supporting Variants
SamplesHG02522
Known GenesST3GAL4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14302966
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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