A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099845



Internal ID21269922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4313515..4422077hg38UCSC Ensembl
Innerchr20:4294162..4402724hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38108563
hg19108563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117199
Supporting Variants
Samplessample145
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099845
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