A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208269



Internal ID22356539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68866111..68868256hg38UCSC Ensembl
chr14:69332828..69334973hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382146
hg192146
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2657n152
Supporting Variantsnssv14444486
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208269
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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