A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090379



Internal ID21999612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72772280..72772280hg38UCSC Ensembl
chr11:72483325..72483325hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596695
Samples
Known GenesSTARD10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090379
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