A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240923



Internal ID22045533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40191966..40191966hg38UCSC Ensembl
chr12:40585768..40585768hg19UCSC Ensembl
Cytoband12q12
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 Variantsnssv17843188
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240923
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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