A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993003



Internal ID21902346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196833466..196852686hg38UCSC Ensembl
chr3:196560337..196579557hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3819221
hg1919221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993003
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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