A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908630



Internal ID22683840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:39951704..41309696hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381357993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv170n209
Supporting Variantsnssv17368474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908630
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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