A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209368



Internal ID22357458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64822374..64822536hg38UCSC Ensembl
chr14:65289092..65289254hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2643n152
Supporting Variantsnssv14444474
SamplesHG00733
Known GenesSPTB
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209368
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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