A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459979



Internal ID22217102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47432566..47432702hg38UCSC Ensembl
chr4:47434583..47434719hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3174054
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)nssv14459979
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer