A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960361



Internal ID22735340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65739040..65739040hg38UCSC Ensembl
chr5:65034867..65034867hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423985
Samples
Known GenesNLN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960361
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer