A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995363



Internal ID21904706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138118374..138119534hg38UCSC Ensembl
chr4:139039528..139040688hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541533
Samples
Known GenesLINC00616, SLC7A11-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995363
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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