A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3189124



Internal ID22340613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:120439938..120446290hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386353
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14407141
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3189124
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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