A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202483



Internal ID22351642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21588033..21597026hg38UCSC Ensembl
chr14:22056152..22065151hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg388994
hg199000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2547n152
Supporting Variantsnssv14381512
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202483
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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