A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220996



Internal ID20788036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17268964..17269807hg38UCSC Ensembl
chr12:17421898..17422741hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38844
hg19844
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587566
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220996
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00044


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