A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9765008



Internal ID18739254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:90564655..90564922hg38UCSC Ensembl
Outerchr5:90564590..90564955hg38UCSC Ensembl
Innerchr5:89860472..89860739hg19UCSC Ensembl
Outerchr5:89860407..89860772hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3566261
Supporting Variants
Samples
Known GenesGPR98
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9765008
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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