A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064397



Internal ID21973630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130765394..130765394hg38UCSC Ensembl
chr3:130484238..130484238hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38825
hg19825
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064397
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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