A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6242785



Internal ID22047395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9387725..9387725hg38UCSC Ensembl
chr19:9498401..9498401hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17849595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6242785
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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