A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227540



Internal ID20794580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20728724..20745010hg38UCSC Ensembl
chr12:20881658..20897944hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg3816287
hg1916287
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583902
Supporting Variants
Samples
Known GenesSLCO1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227540
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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