A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731739



Internal ID20507660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50451564..50451637hg38UCSC Ensembl
chr19:50954821..50954894hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265267
Samples
Known GenesMYBPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731739
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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