A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6250985



Internal ID22055595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29719335..29719335hg38UCSC Ensembl
chr19:30210242..30210242hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6250985
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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