A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111455



Internal ID22020689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34742662..34742662hg38UCSC Ensembl
chr18:32322626..32322626hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635496
Samples
Known GenesDTNA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111455
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