A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974890



Internal ID22749825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60424267..60424267hg38UCSC Ensembl
chr15:60716466..60716466hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376859
Samples
Known GenesNARG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974890
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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