A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102245



Internal ID22011480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15032020..15032020hg38UCSC Ensembl
chr21:16404341..16404341hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637962
Samples
Known GenesNRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102245
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