A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099477



Internal ID21290704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:12307235..12311814hg38UCSC Ensembl
Innerchr18:12307234..12311813hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg384580
hg194580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112456
Supporting Variants
Samplessample62
Known GenesTUBB6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099477
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