A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860887



Internal ID22635822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137952071..138002399hg38UCSC Ensembl
chr9:140846523..140896851hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3850329
hg1950329
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511851
Samples
Known GenesCACNA1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860887
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