A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107495



Internal ID21266960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94472228..94492666hg38UCSC Ensembl
Innerchr1:94937784..94958222hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3820439
hg1920439
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112760
Supporting Variants
Samplessample105
Known GenesABCD3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107495
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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