A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218438



Internal ID20785478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16659439..16662254hg38UCSC Ensembl
chr12:16812373..16815188hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg382816
hg192816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586938
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218438
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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