A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193892



Internal ID22344282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20783735..20783915hg38UCSC Ensembl
chr14:21251894..21252074hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14444935
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)nsv3193892
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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