A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226009



Internal ID20793049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52940159..52940798hg38UCSC Ensembl
chr12:53333943..53334582hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582464
Supporting Variants
Samples
Known GenesKRT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226009
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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