A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3179161



Internal ID22335401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3357548..3357650hg38UCSC Ensembl
chr1:3274112..3274214hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390094
SamplesNA19240
Known GenesPRDM16
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3179161
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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