A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv394n223



Internal ID22803362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157093509..157094912hg38UCSC Ensembl
chr1:157063301..157064704hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381404
hg191404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6538631, nsv6543034
Samples
Known GenesETV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv394n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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