A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094653



Internal ID21283677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70703885..70706483hg38UCSC Ensembl
Innerchr4:71569602..71572200hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg382599
hg192599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112809
Supporting Variants
Samplessample348
Known GenesRUFY3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094653
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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