A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv746n209



Internal ID22826821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38751320..38771167hg38UCSC Ensembl
chr15:39043521..39063368hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3819848
hg1919848
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5865681, nsv5851334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv746n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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