A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6250996



Internal ID22055606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31587201..31587201hg38UCSC Ensembl
chr19:32078107..32078107hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6250996
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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