A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241381



Internal ID22045991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240618200..240618200hg38UCSC Ensembl
chr1:240781500..240781500hg19UCSC Ensembl
Cytoband1q43
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 Variantsnssv17845005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241381
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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