A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222128



Internal ID20789168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50499941..50501581hg38UCSC Ensembl
chr12:50893724..50895364hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg381641
hg191641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590485
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222128
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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