A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089429



Internal ID21268967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:47632193..47635394hg38UCSC Ensembl
Innerchr4:47634210..47637411hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg383202
hg193202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116193
Supporting Variants
Samplessample133
Known GenesCORIN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089429
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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