A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909287



Internal ID22684497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117759538..117763477hg38UCSC Ensembl
chr10:119519049..119522988hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383940
hg193940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909287
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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