A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886337



Internal ID22661324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62652299..62655580hg38UCSC Ensembl
chr18:60319532..60322813hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383282
hg193282
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886337
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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