A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915841



Internal ID22691059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84640335..84666732hg38UCSC Ensembl
chr10:86400091..86426488hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3826398
hg1926398
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915841
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