A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752178



Internal ID18726424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:52259669..52260458hg38UCSC Ensembl
Outerchr16:52259589..52260502hg38UCSC Ensembl
Innerchr16:52293581..52294370hg19UCSC Ensembl
Outerchr16:52293501..52294414hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38914
hg19914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553431
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752178
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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