A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14178522



Internal ID4180338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61881703..61885743hg38UCSC Ensembl
Innerchr11:61881707..61885739hg38UCSC Ensembl
Outerchr11:61881699..61885747hg38UCSC Ensembl
chr11:61649175..61653215hg19UCSC Ensembl
Innerchr11:61649179..61653211hg19UCSC Ensembl
Outerchr11:61649171..61653219hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg384041
hg194041
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626586
Supporting Variants
SamplesNA19471
Known GenesFADS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14178522
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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