A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3186620



Internal ID22339296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43541207..43542112hg38UCSC Ensembl
chr5:43541309..43542214hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7311n152
Supporting Variantsnssv14425652
SamplesHG00514
Known GenesPAIP1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3186620
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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