A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5410871



Internal ID190186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88208025..88208059hg38UCSC Ensembl
chr5:87503842..87503876hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968832
Samples
Known GenesTMEM161B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5410871
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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