A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866829



Internal ID22641764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42906446..42916869hg38UCSC Ensembl
chr9:44054250..44064673hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3810424
hg1910424
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513512, nssv17513511
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866829
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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