A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925852



Internal ID22701079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76292323..76294400hg38UCSC Ensembl
chr10:78052081..78054158hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382078
hg192078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365035
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925852
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