A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853109



Internal ID22628044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66891571..66893303hg38UCSC Ensembl
chr9:40799538..40801270hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg381733
hg191733
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514064, nssv17514065, nssv17514063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853109
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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