A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3553584



Internal ID18754660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65486112..65486377hg38UCSC Ensembl
Outerchr16:65486068..65486451hg38UCSC Ensembl
Innerchr16:65520015..65520280hg19UCSC Ensembl
Outerchr16:65519971..65520354hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9752331
Samples
Known GenesLINC00922
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3553584
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer