A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081171



Internal ID21990404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75068436..75068436hg38UCSC Ensembl
chr9:77683352..77683352hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383416
hg193416
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586717
Samples
Known GenesNMRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081171
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