A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449693



Internal ID227923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172029445..172031269hg38UCSC Ensembl
chr3:171747235..171749059hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381825
hg191825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943185
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449693
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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