A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744073



Internal ID18371633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111911905..111911962hg38UCSC Ensembl
chr9:114674185..114674242hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545326
Supporting Variants
Samples
Known GenesUGCG
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744073
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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