A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231508



Internal ID20798548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11809021..11809992hg38UCSC Ensembl
chr12:11961955..11962926hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588144
Supporting Variants
Samples
Known GenesETV6, RNU6-19P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231508
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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