A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092261



Internal ID22001494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59217922..59217922hg38UCSC Ensembl
chr11:58985395..58985395hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092261
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