A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359460



Internal ID22585129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89347241..89363801hg38UCSC Ensembl
chr10:91106998..91123558hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3816561
hg1916561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910314
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359460
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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