A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741129



Internal ID20517106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2296870..2296996hg38UCSC Ensembl
chr19:2296869..2296995hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266550
Samples
Known GenesLINGO3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741129
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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