A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733187



Internal ID20509115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48751603..48751741hg38UCSC Ensembl
chr19:49254860..49254998hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271457
Samples
Known GenesFUT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733187
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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