A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv516n223



Internal ID22803484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207105279..207106736hg38UCSC Ensembl
chr1:207278624..207280081hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381458
hg191458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6554793, nsv6543379
Samples
Known GenesC4BPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv516n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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