A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869452



Internal ID22644387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11303378..11305791hg38UCSC Ensembl
chrUn_gl000234:16392..18805hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382414
hg192414
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488998, nssv17480997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869452
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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