A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073961



Internal ID21983194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191736719..191736719hg38UCSC Ensembl
chr3:191454508..191454508hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073961
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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