A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995191



Internal ID21904534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138089453..138089800hg38UCSC Ensembl
chr4:139010607..139010954hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546129
Samples
Known GenesLINC00616, SLC7A11-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995191
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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