A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14429912



Internal ID22171823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90455194..90455270hg38UCSC Ensembl
chr14:90921538..90921614hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190552
Supporting Variants
SamplesHG00514
Known GenesLINC00642
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14429912
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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