A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199920



Internal ID22349441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101970149..101970842hg38UCSC Ensembl
chr14:102436486..102437179hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459786
SamplesHG00733
Known GenesDYNC1H1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199920
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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