A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14429910



Internal ID22171821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89511185..89511238hg38UCSC Ensembl
chr14:89977529..89977582hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221994
Supporting Variants
SamplesHG00514
Known GenesFOXN3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14429910
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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