A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226748



Internal ID20793788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21692689..21866315hg38UCSC Ensembl
chr12:21845623..22019249hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38173627
hg19173627
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591644
Supporting Variants
Samples
Known GenesABCC9, KCNJ8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226748
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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