A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464286



Internal ID242167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95408153..95410043hg38UCSC Ensembl
chr5:94743857..94745747hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381891
hg191891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16972388
Samples
Known GenesFAM81B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464286
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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