A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218836



Internal ID20785876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62710305..62711242hg38UCSC Ensembl
chr12:63104085..63105022hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587415
Supporting Variants
Samples
Known GenesPPM1H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218836
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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