A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870463



Internal ID22645399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11596288..11604769hg38UCSC Ensembl
chrUn_gl000231:10299..18780hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388482
hg198482
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489017, nssv17489018
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870463
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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