A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752056



Internal ID18726302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:29713680..29730075hg38UCSC Ensembl
Outerchr16:29709708..29734179hg38UCSC Ensembl
Innerchr16:29725001..29741396hg19UCSC Ensembl
Outerchr16:29721029..29745500hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3824472
hg1924472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553309
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752056
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