A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5405028



Internal ID184373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114823059..114823059hg38UCSC Ensembl
chr10:116582818..116582818hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039226
Samples
Known GenesFAM160B1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5405028
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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