A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757046



Internal ID20532906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18116779..18116779hg38UCSC Ensembl
chr19:18227589..18227589hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265993
Samples
Known GenesMAST3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757046
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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