A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094656



Internal ID21283675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99945437..99947397hg38UCSC Ensembl
Innerchr4:100866594..100868554hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381961
hg191961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110532
Supporting Variants
Samplessample348
Known GenesDNAJB14
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094656
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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