A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094661



Internal ID21283746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:165726572..165738295hg38UCSC Ensembl
Innerchr4:166647724..166659447hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3811724
hg1911724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114946
Supporting Variants
Samplessample349
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094661
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