A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2097n209



Internal ID22828172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31731559..31739144hg38UCSC Ensembl
chr9:31731557..31739142hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg387586
hg197586
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5858501, nsv5863875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2097n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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