A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752034



Internal ID18379594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27325338..27339679hg38UCSC Ensembl
Outerchr16:27324680..27341801hg38UCSC Ensembl
Innerchr16:27336659..27351000hg19UCSC Ensembl
Outerchr16:27336001..27353122hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3817122
hg1917122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553287
Supporting Variants
Samples
Known GenesIL4R
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752034
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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