A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219691



Internal ID20786731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56760050..56761280hg38UCSC Ensembl
chr12:57153834..57155064hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219691
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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