A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859108



Internal ID22634043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60885015..60889550hg38UCSC Ensembl
chr9:41471287..41475822hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg384536
hg194536
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513768, nssv17513769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859108
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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