A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090461



Internal ID21270271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48482589..48486919hg38UCSC Ensembl
Innerchr4:48484606..48488936hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg384331
hg194331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112227
Supporting Variants
Samplessample149
Known GenesSLC10A4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090461
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