A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223885



Internal ID20790925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66057681..66281138hg38UCSC Ensembl
chr12:66451461..66674918hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38223458
hg19223458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577462
Supporting Variants
Samples
Known GenesIRAK3, LLPH, TMBIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223885
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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