A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965366



Internal ID22740301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138599167..138599167hg38UCSC Ensembl
chr7:138283912..138283912hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442994
Samples
Known GenesSVOPL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965366
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