A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090703



Internal ID21272898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178721442..179029513hg38UCSC Ensembl
Innerchr4:179642596..179950667hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38308072
hg19308072
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112676
Supporting Variants
Samplessample184
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090703
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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