A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14450603



Internal ID22245756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171555858..171556151hg38UCSC Ensembl
chr3:171273648..171273941hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179233
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)nssv14450603
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