A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760769



Internal ID20536629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50459523..50459523hg38UCSC Ensembl
chr19:50962780..50962780hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267225
Samples
Known GenesMYBPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760769
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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