A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925028



Internal ID22700255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64339300..64493267hg38UCSC Ensembl
chr10:66099060..66253024hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38153968
hg19153965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925028
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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