A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251891



Internal ID20818931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86066257..86067115hg38UCSC Ensembl
chr1:86531940..86532798hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547112
Supporting Variants
Samples
Known GenesCOL24A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251891
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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