A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850586



Internal ID22625521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90410529..90412895hg38UCSC Ensembl
chr9:93172811..93175177hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382367
hg192367
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850586
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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