A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752361



Internal ID18726607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69325359..69325426hg38UCSC Ensembl
Outerchr16:69325358..69325427hg38UCSC Ensembl
Innerchr16:69359262..69359329hg19UCSC Ensembl
Outerchr16:69359261..69359330hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553614
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752361
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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