A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099895



Internal ID22009128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58053632..58053632hg38UCSC Ensembl
chr11:57821104..57821104hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595667
Samples
Known GenesOR9Q1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099895
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