A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252844



Internal ID20819884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10432612..10433075hg38UCSC Ensembl
chr20:10413260..10413723hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595702
Supporting Variants
Samples
Known GenesMKKS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252844
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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