A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7516619



Internal ID10794901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113802585..113803665hg38UCSC Ensembl
Outerchr13:114505558..114506638hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3247052
Supporting Variants
SamplesHuRef
Known GenesTMEM255B
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7516619
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