A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193631



Internal ID22344059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104051786..104052052hg38UCSC Ensembl
chr14:104518123..104518389hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14417220
SamplesHG00514
Known GenesTDRD9
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193631
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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