A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752253



Internal ID18726499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58993852..58994226hg38UCSC Ensembl
Outerchr16:58993758..58994291hg38UCSC Ensembl
Innerchr16:59027756..59028130hg19UCSC Ensembl
Outerchr16:59027662..59028195hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752253
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