A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv36n199



Internal ID22802922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44854527..45034654hg38UCSC Ensembl
chr15:45146725..45326852hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38180128
hg19180128
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4753087, nsv4752719
Samples
Known GenesC15orf43, SORD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv36n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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