A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026821



Internal ID21936164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113955527..113955952hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026821
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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