A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447477



Internal ID225780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186174976..186183860hg38UCSC Ensembl
chr3:185892765..185901649hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg388885
hg198885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944852
Samples
Known GenesDGKG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447477
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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