A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970542



Internal ID22745477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17450797..17450797hg38UCSC Ensembl
chr19:17561606..17561606hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970542
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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