A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100939



Internal ID22010172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56650881..56650881hg38UCSC Ensembl
chr18:54318112..54318112hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100939
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