A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439555



Internal ID218090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194948879..194949027hg38UCSC Ensembl
chr3:194669608..194669756hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439555
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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