A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555099



Internal ID21879454
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 StatusS
Merged Variantsnsv5997187
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555099
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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