A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872416



Internal ID22647356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48472908..48480175hg38UCSC Ensembl
chr18:45999279..46006546hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg387268
hg197268
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478519
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872416
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer