A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240619



Internal ID22045229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43786388..43786388hg38UCSC Ensembl
chr10:44281836..44281836hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240619
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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