A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848790



Internal ID22623725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88415720..88424174hg38UCSC Ensembl
chr9:91030635..91039089hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg388455
hg198455
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514681
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848790
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