A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220406



Internal ID20787446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30178915..30184224hg38UCSC Ensembl
chr12:30331848..30337157hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg385310
hg195310
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580719
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220406
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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