A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363600



Internal ID22589269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41056563..41265070hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38208508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921659
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363600
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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