A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233929



Internal ID20800970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89642587..89644157hg38UCSC Ensembl
chr12:90036364..90037934hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg381571
hg191571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595449
Supporting Variants
Samples
Known GenesATP2B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233929
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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