A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889083



Internal ID22664095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170173024..170173291hg38UCSC Ensembl
chr3:169890812..169891079hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425787
Samples
Known GenesPHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889083
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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