A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7452246



Internal ID10383842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88933336..88933777hg38UCSC Ensembl
Outerchr16:88999744..89000185hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3182679
Supporting Variants
SamplesHuRef
Known GenesCBFA2T3
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7452246
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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