A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450169



Internal ID228386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137782984..137783038hg38UCSC Ensembl
chr3:137501826..137501880hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450169
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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