A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856088



Internal ID22631023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81949158..81951200hg38UCSC Ensembl
chr9:84564073..84566115hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg382043
hg192043
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514442
Samples
Known GenesSPATA31D3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856088
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