A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444387



Internal ID222760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172318787..172320141hg38UCSC Ensembl
chr3:172036577..172037931hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943205
Samples
Known GenesFNDC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444387
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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