A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995516



Internal ID21904859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155452121..155452953hg38UCSC Ensembl
chr4:156373273..156374105hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995516
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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