A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222759



Internal ID20789799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122393182..122393928hg38UCSC Ensembl
chr12:122877729..122878475hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592992
Supporting Variants
Samples
Known GenesCLIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222759
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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