A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960421



Internal ID22735394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49994034..49994093hg38UCSC Ensembl
chr22:50432463..50432522hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960421
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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