A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062888



Internal ID21972121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32475236..32475236hg38UCSC Ensembl
chr3:32516728..32516728hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062888
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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