A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3189831



Internal ID22340979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:12685829..12705964hg38UCSC Ensembl
chr5:12685941..12706076hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3820136
hg1920136
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14398600
SamplesNA19240
Known GenesCT49
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3189831
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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