A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082706



Internal ID21991939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:131217..131217hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622077
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082706
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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