A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107608



Internal ID22016841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30511696..30511696hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38442
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107608
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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