A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250074



Internal ID20817114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:239044109..239045745hg38UCSC Ensembl
chr1:239207409..239209045hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg381637
hg191637
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250074
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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