A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14450596



Internal ID22245749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169769250..169769399hg38UCSC Ensembl
chr3:169487038..169487187hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3173867
Supporting Variants
SamplesHG00733
Known GenesACTRT3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14450596
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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