A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884558



Internal ID22659541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38835466..38846093hg38UCSC Ensembl
chr18:36415430..36426057hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3810628
hg1910628
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884558
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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