A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761912



Internal ID20537772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13936856..13936856hg38UCSC Ensembl
chr19:14047669..14047669hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278856
Samples
Known GenesPODNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761912
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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