A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226159



Internal ID20793199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51332628..51333110hg38UCSC Ensembl
chr12:51726412..51726894hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588484
Supporting Variants
Samples
Known GenesCELA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226159
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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