A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103814



Internal ID22013047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57741237..57741237hg38UCSC Ensembl
chr20:56316293..56316293hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103814
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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