A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744293



Internal ID20520291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57425465..57425631hg38UCSC Ensembl
chr19:57936833..57936999hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744293
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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