A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103761



Internal ID21266776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:143835616..143839122hg38UCSC Ensembl
Innerchr2:144593185..144596691hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg383507
hg193507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110827
Supporting Variants
Samplessample102
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103761
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