A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446434



Internal ID21103987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137861588..137908119hg38UCSC Ensembl
chr9:140756040..140802571hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3846532
hg1946532
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234019
Samples
Known GenesCACNA1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446434
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer