A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227923



Internal ID20794963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111651458..111651656hg38UCSC Ensembl
chr12:112089262..112089460hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583953
Supporting Variants
Samples
Known GenesBRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227923
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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