A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14423047



Internal ID22161850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73802064..73802391hg38UCSC Ensembl
chr3:73851215..73851542hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3182329
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14423047
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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