A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061297



Internal ID21970530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32002733..32002733hg38UCSC Ensembl
chr3:32044225..32044225hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061297
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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