A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914817



Internal ID22690034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41098317..41108748hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3810432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914817
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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