A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6242800



Internal ID22047410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14337507..14337507hg38UCSC Ensembl
chr19:14448319..14448319hg19UCSC Ensembl
Cytoband19p13.12
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 Variantsnssv17849610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6242800
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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