A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv99n209



Internal ID22826174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154980038..154982391hg38UCSC Ensembl
chr1:154952514..154954867hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382354
hg192354
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5828040, nsv5828039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv99n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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