A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853531



Internal ID22628466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28887013..28892196hg38UCSC Ensembl
chr9:28887011..28892194hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg385184
hg195184
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512673
Samples
Known GenesLINGO2, MIR873
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853531
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