A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866411



Internal ID22641346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131967365..131972714hg38UCSC Ensembl
chr9:134842752..134848101hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg385350
hg195350
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511610
Samples
Known GenesMED27
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866411
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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