A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097051



Internal ID22006284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49403014..49403014hg38UCSC Ensembl
chr17:47480376..47480376hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097051
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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