A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093557



Internal ID21281586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26283968..26294888hg38UCSC Ensembl
Innerchr4:26285590..26296510hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3810921
hg1910921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111981
Supporting Variants
Samplessample313
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093557
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