A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040749



Internal ID21950088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3321631..3321631hg38UCSC Ensembl
chr3:3363315..3363315hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519058
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040749
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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