A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885371



Internal ID22660355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58778138..58783552hg38UCSC Ensembl
chr18:56445370..56450784hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg385415
hg195415
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885371
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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