A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067782



Internal ID21977015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42937015..42937015hg38UCSC Ensembl
chr3:42978507..42978507hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548399
Samples
Known GenesKRBOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067782
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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