A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5440774



Internal ID219273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58624298..58647277hg38UCSC Ensembl
chr3:58610025..58633004hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3822980
hg1922980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933031
Samples
Known GenesFAM107A, FAM3D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5440774
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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