A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090372



Internal ID21999605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56460009..56460009hg38UCSC Ensembl
chr15:56752207..56752207hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606679
Samples
Known GenesMNS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090372
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