A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259027



Internal ID22063637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70194644..70194644hg38UCSC Ensembl
chr17:68190785..68190785hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259027
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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