A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438620



Internal ID217180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49849448..49852616hg38UCSC Ensembl
chr3:49886881..49890049hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383169
hg193169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933375
Samples
Known GenesTRAIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438620
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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