A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv47n199



Internal ID22802933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60020856..60125691hg38UCSC Ensembl
chr17:58098217..58203052hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38104836
hg19104836
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4764279, nsv4760208
Samples
Known GenesHEATR6, LOC645638, LOC653653, MIR4737
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv47n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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