A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv877n223



Internal ID22803845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103304895..103307094hg38UCSC Ensembl
chr10:105064652..105066851hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6592387, nsv6581762
Samples
Known GenesPCGF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv877n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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