A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14453305



Internal ID22248079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101723090..101726052hg38UCSC Ensembl
chr14:102189427..102192389hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg382963
hg192963
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201422
Supporting Variants
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)nssv14453305
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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