A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764517



Internal ID20540377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52853599..52853599hg38UCSC Ensembl
chr19:53356852..53356852hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264038
Samples
Known GenesZNF468
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764517
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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