A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424328



Internal ID203323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14208769..14208820hg38UCSC Ensembl
chr19:14319581..14319632hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721665
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424328
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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