A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14435277



Internal ID22178182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45335169..45335325hg38UCSC Ensembl
chr3:45376661..45376817hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3187533
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)nssv14435277
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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