A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851038



Internal ID22625973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88477115..88479972hg38UCSC Ensembl
chr9:91092030..91094887hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg382858
hg192858
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514701
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851038
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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