A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5470086



Internal ID247857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:161906711..162030123hg38UCSC Ensembl
chr4:162827863..162951275hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38123413
hg19123413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16957731
Samples
Known GenesFSTL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5470086
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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