A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2855791



Internal ID10875488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:81765055..81765598hg38UCSC Ensembl
Outerchr16:81798660..81799203hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7125358
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2855791
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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