A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995462



Internal ID21904805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148622949..148628929hg38UCSC Ensembl
chr4:149544101..149550081hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg385981
hg195981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555558
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995462
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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