A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1442n209



Internal ID22827517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4428825..4439749hg38UCSC Ensembl
chr3:4470509..4481433hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3810925
hg1910925
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5836278, nsv5835996
Samples
Known GenesSUMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1442n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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