A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113781



Internal ID21297047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:231707073..231711229hg38UCSC Ensembl
Innerchr2:232571783..232575939hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg384157
hg194157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106751
Samplessample363
Known GenesPTMA
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113781
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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