A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14450602



Internal ID22245755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170777247..170777628hg38UCSC Ensembl
chr3:170495036..170495417hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3186771
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14450602
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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