A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996401



Internal ID21905744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18840383..18841480hg38UCSC Ensembl
chr4:18842006..18843103hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg381098
hg191098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545920
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996401
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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