A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870819



Internal ID22645756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47489043..47496093hg38UCSC Ensembl
chr18:45015414..45022464hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg387051
hg197051
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478510
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870819
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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