A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217930



Internal ID20784970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66033387..66034054hg38UCSC Ensembl
chr12:66427167..66427834hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586292
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217930
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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