A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3155800



Internal ID10828781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114526438..114526508hg38UCSC Ensembl
chr11:114397160..114397230hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7425367
SamplesHuRef
Known GenesNXPE1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3155800
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