A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2862235



Internal ID10881932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:119525206..119525568hg38UCSC Ensembl
Outerchr2:120282782..120283144hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7131802
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2862235
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