A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353429



Internal ID22579098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110144092..110146480hg38UCSC Ensembl
chr10:111903850..111906238hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382389
hg192389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915939
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353429
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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