A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883257



Internal ID22658235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87944729..87950040hg38UCSC Ensembl
chr16:87978335..87983646hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg385312
hg195312
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474160
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883257
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