A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869542



Internal ID22644477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33767468..33773946hg38UCSC Ensembl
chr18:31347432..31353910hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg386479
hg196479
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479615
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869542
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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