A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227269



Internal ID20794309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89435504..89436528hg38UCSC Ensembl
chr12:89829281..89830305hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg381025
hg191025
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588444
Supporting Variants
Samples
Known GenesPOC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227269
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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