A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv98n209



Internal ID22826173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154666558..154669257hg38UCSC Ensembl
chr1:154639034..154641733hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5828361, nsv5828360
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv98n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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