A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104559



Internal ID22013792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22973335..22973335hg38UCSC Ensembl
chr20:22953972..22953972hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104559
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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