A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465359



Internal ID243221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158353000..158363381hg38UCSC Ensembl
chr4:159274152..159284533hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3810382
hg1910382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16958863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465359
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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