A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100955



Internal ID21287430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11576463..11584276hg38UCSC Ensembl
Innerchr18:11576462..11584275hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg387814
hg197814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114765
Supporting Variants
Samplessample400
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100955
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