A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101955



Internal ID21270608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19019387..19022547hg38UCSC Ensembl
Innerchr21:20391706..20394866hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg383161
hg193161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117538
Supporting Variants
Samplessample153
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101955
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