A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926606



Internal ID22701833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130135713..130135849hg38UCSC Ensembl
chr10:131933977..131934113hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926606
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