A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998044



Internal ID21907387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68233048..68233169hg38UCSC Ensembl
chr4:69098766..69098887hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544863
Samples
Known GenesTMPRSS11B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998044
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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