A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998885



Internal ID21908228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88828061..88829056hg38UCSC Ensembl
chr4:89749212..89750207hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38996
hg19996
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546963
Samples
Known GenesFAM13A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998885
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer