A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234159



Internal ID20801199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64733298..66057590hg38UCSC Ensembl
chr12:65127078..66451370hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg381324293
hg191324293
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576953
Supporting Variants
Samples
Known GenesFLJ41278, GNS, HMGA2, LEMD3, MIR6074, MSRB3, RPSAP52, TBC1D30, WIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234159
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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