A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103843



Internal ID22013076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62349820..62349820hg38UCSC Ensembl
chr20:60924876..60924876hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38904
hg19904
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622669
Samples
Known GenesLAMA5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103843
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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