A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996239



Internal ID21905582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164330115..165027122hg38UCSC Ensembl
chr4:165251267..165948274hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38697008
hg19697008
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540903
Samples
Known GenesFAM218A, LOC100505989, LOC100506013, MARCH1, MIR5684, TRIM61
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996239
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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