A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv506n223



Internal ID22803474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197787392..197789087hg38UCSC Ensembl
chr1:197756522..197758217hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg381696
hg191696
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6537276, nsv6541503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv506n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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