A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081473



Internal ID21990706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5076495..5076495hg38UCSC Ensembl
chr17:4979790..4979790hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081473
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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