A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082424



Internal ID21991657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46983464..46983464hg38UCSC Ensembl
chr17:45060830..45060830hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618088
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082424
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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