A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885894



Internal ID22660880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4684250..4687609hg38UCSC Ensembl
chr18:4684250..4687609hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383360
hg193360
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478497, nssv17478498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885894
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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