A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219729



Internal ID20786769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68778836..68780288hg38UCSC Ensembl
chr12:69172616..69174068hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg381453
hg191453
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585833
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219729
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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