A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6253741



Internal ID22058351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16735824..16735824hg38UCSC Ensembl
chr3:16777331..16777331hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17854788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6253741
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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