A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854110



Internal ID22629045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132999919..133003229hg38UCSC Ensembl
chr9:135875306..135878616hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg383311
hg193311
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854110
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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