A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105406



Internal ID21267776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126989138..127036481hg38UCSC Ensembl
Innerchr3:126707981..126755324hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3847344
hg1947344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118295
Supporting Variants
Samplessample116
Known GenesPLXNA1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105406
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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