A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3553914



Internal ID18408304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89830022..89831792hg38UCSC Ensembl
Outerchr16:89829577..89832023hg38UCSC Ensembl
Innerchr16:89896430..89898200hg19UCSC Ensembl
Outerchr16:89895985..89898431hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382447
hg192447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9752661
Samples
Known GenesSPIRE2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3553914
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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