A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093341



Internal ID21278649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32672983..32681027hg38UCSC Ensembl
Innerchr4:32674605..32682649hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg388045
hg198045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111827
Supporting Variants
Samplessample272
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093341
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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