A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970058



Internal ID22744993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2659082..2659082hg38UCSC Ensembl
chr20:2639728..2639728hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403882
Samples
Known GenesIDH3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970058
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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