A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738288



Internal ID20514256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68552660..68552990hg38UCSC Ensembl
chr17:66548801..66549131hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259905
Samples
Known GenesFAM20A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738288
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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