A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3173867



Internal ID22332522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169769250..169769399hg38UCSC Ensembl
chr3:169487038..169487187hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14423608, nssv14450596
SamplesHG00733, HG00514
Known GenesACTRT3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3173867
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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