A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv45n199



Internal ID22802931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43227252..43389474hg38UCSC Ensembl
chr17:41379299..41466842hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38162223
hg1987544
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4759534, nsv4761353, nsv4759053, nsv4756332, nsv4765955, nsv4757351, nsv4757545
Samples
Known GenesLINC00854, LINC00910
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv45n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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