A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953839



Internal ID22697259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63596339..63596339hg38UCSC Ensembl
chr10:65356099..65356099hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351935
Samples
Known GenesREEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953839
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