A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866180



Internal ID22641115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43005818..43034056hg38UCSC Ensembl
chr9:42949208..42977448hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3828239
hg1928241
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513564, nssv17513565
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866180
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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