A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866379



Internal ID22641314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64107621..64111688hg38UCSC Ensembl
chrUn_gl000211:139174..143241hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384068
hg194068
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513969, nssv17513970
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866379
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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