A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973900



Internal ID22748835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123099951..123099951hg38UCSC Ensembl
chr10:124859467..124859467hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355691
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973900
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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