A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234199



Internal ID20801239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92275361..92277291hg38UCSC Ensembl
chr12:92669137..92671067hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381931
hg191931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580732
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234199
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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