A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101841



Internal ID21271891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:216033903..216039648hg38UCSC Ensembl
Innerchr2:216898626..216904371hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg385746
hg195746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114161
Supporting Variants
Samplessample17
Known GenesPECR
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101841
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