A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880296



Internal ID22655266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11298961..11301880hg38UCSC Ensembl
chrUn_gl000234:20303..23224hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382920
hg192922
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488997, nssv17480996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880296
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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