A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998926



Internal ID21908269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97105303..97682590hg38UCSC Ensembl
chr4:98026454..98603741hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38577288
hg19577288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556374
Samples
Known GenesSTPG2, STPG2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998926
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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