A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763919



Internal ID18738165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184697354..184697426hg38UCSC Ensembl
chr4:185618508..185618580hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3565172
Supporting Variants
Samples
Known GenesCENPU
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763919
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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