A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9747171



Internal ID18374731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120121911..120121986hg38UCSC Ensembl
chr11:119992619..119992694hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3548424
Supporting Variants
Samples
Known GenesTRIM29
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9747171
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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