A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107548



Internal ID21291588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178189609..178944992hg38UCSC Ensembl
Innerchr4:179110763..179866146hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38755384
hg19755384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117207
Supporting Variants
Samplessample77
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107548
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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