A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914896



Internal ID22690113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:39963932..41194270hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381230339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv170n209
Supporting Variantsnssv17356699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914896
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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