A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762890



Internal ID20538750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43665720..43665720hg38UCSC Ensembl
chr19:44169872..44169872hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287048
Samples
Known GenesPLAUR
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762890
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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