A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14466074



Internal ID22234569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93768967..93769023hg38UCSC Ensembl
chr14:94235313..94235369hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204879
Supporting Variants
SamplesHG00733
Known GenesPRIMA1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14466074
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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