A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997187



Internal ID21906530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38807771..38807952hg38UCSC Ensembl
chr4:38809392..38809573hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997187
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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