A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106371



Internal ID21269390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178592159..178594612hg38UCSC Ensembl
Innerchr3:178309947..178312400hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg382454
hg192454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114682
Supporting Variants
Samplessample138
Known GenesKCNMB2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106371
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