A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236086



Internal ID20803126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120780335..120781746hg38UCSC Ensembl
chr12:121218138..121219549hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381412
hg191412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576989
Supporting Variants
Samples
Known GenesSPPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236086
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00022


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