A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866457



Internal ID22641392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125037974..125042098hg38UCSC Ensembl
chr9:127800253..127804377hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384125
hg194125
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511344
Samples
Known GenesSCAI
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866457
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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