A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199841



Internal ID22349377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3111181..3111240hg38UCSC Ensembl
chr16:3161182..3161241hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14453492
SamplesHG00733
Known GenesZNF205-AS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199841
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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