A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249722



Internal ID22054332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60478840..60478840hg38UCSC Ensembl
chr15:60771039..60771039hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846825
Samples
Known GenesNARG2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249722
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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