A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093365



Internal ID21278969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:47810539..47826778hg38UCSC Ensembl
Innerchr4:47812556..47828795hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3816240
hg1916240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117410
Supporting Variants
Samplessample276
Known GenesCORIN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093365
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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