A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231712



Internal ID20798752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92066801..92067633hg38UCSC Ensembl
chr12:92460577..92461409hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579907
Supporting Variants
Samples
Known GenesC12orf79
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231712
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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