A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5411489



Internal ID190796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98531743..98531785hg38UCSC Ensembl
chr4:99452894..99452936hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954273
Samples
Known GenesTSPAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5411489
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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