A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227885



Internal ID20794925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2869549..2870680hg38UCSC Ensembl
chr12:2978715..2979846hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg381132
hg191132
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583322
Supporting Variants
Samples
Known GenesFOXM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227885
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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