A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867726



Internal ID22642662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:16184452..16207105hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3822654
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481422, nssv17481423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867726
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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