A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061176



Internal ID21970409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149301456..149301456hg38UCSC Ensembl
chr3:149019243..149019243hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061176
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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