A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877328



Internal ID22652292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45760935..45768137hg38UCSC Ensembl
chr18:43340900..43348102hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg387203
hg197203
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478486
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877328
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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