A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849610



Internal ID22033253
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 StatusS
Merged Variantsnsv6242800
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849610
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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