A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14418400



Internal ID22155047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10884130..10885135hg38UCSC Ensembl
chr16:10977987..10978992hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381006
hg191006
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201022
Supporting Variants
SamplesHG00514
Known GenesCIITA
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14418400
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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