A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3186569



Internal ID22339273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19642980..19643124hg38UCSC Ensembl
chr1:19969474..19969618hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14384431
SamplesNA19240
Known GenesMINOS1-NBL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3186569
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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