A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2149n209



Internal ID22828224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82754234..82772194hg38UCSC Ensembl
chr9:85369149..85387109hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3817961
hg1917961
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5862783, nsv5863986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2149n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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