A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093475



Internal ID21280321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102748237..102752376hg38UCSC Ensembl
Innerchr4:103669394..103673533hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg384140
hg194140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114937
Supporting Variants
Samplessample296
Known GenesMANBA
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093475
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