A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106151



Internal ID22015384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53254660..53254660hg38UCSC Ensembl
chr18:50781030..50781030hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629061
Samples
Known GenesDCC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106151
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