A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103435



Internal ID22012670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2659082..2659082hg38UCSC Ensembl
chr20:2639728..2639728hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622358
Samples
Known GenesIDH3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103435
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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