A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992805



Internal ID21902148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197773971..197774032hg38UCSC Ensembl
chr3:197500842..197500903hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550451
Samples
Known GenesFYTTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992805
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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