A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736112



Internal ID20512057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14523373..14523454hg38UCSC Ensembl
chr19:14634185..14634266hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736112
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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