A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423762



Internal ID202774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16075538..16075589hg38UCSC Ensembl
chr19:16186348..16186399hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721837
Samples
Known GenesTPM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423762
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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