A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6254181



Internal ID22058791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70584190..70584190hg38UCSC Ensembl
chr3:70633341..70633341hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17854059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6254181
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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