A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228826



Internal ID20795866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40132474..40134022hg38UCSC Ensembl
chr12:40526276..40527824hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg381549
hg191549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594467
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228826
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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