A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881078



Internal ID22656051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45761860..45765133hg38UCSC Ensembl
chr18:43341825..43345098hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg383274
hg193274
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881078
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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