A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099892



Internal ID22009125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137889087..137889087hg38UCSC Ensembl
chr9:140783539..140783539hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582462
Samples
Known GenesCACNA1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099892
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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