A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862179



Internal ID22637114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96618134..96619233hg38UCSC Ensembl
chr9:99380416..99381515hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514923, nssv17514924
Samples
Known GenesCDC14B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862179
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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