A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226287



Internal ID20793327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120279817..120280598hg38UCSC Ensembl
chr12:120717620..120718401hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226287
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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