A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv508n223



Internal ID22803476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200011111..200013712hg38UCSC Ensembl
chr1:199980239..199982840hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382602
hg192602
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6536030, nsv6548340
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv508n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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