A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996778



Internal ID21906121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18119247..18125804hg38UCSC Ensembl
chr4:18120870..18127427hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg386558
hg196558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556514
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996778
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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