A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14436519



Internal ID22179667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5835666..5835947hg38UCSC Ensembl
chr6:5835899..5836180hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3188980
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)nssv14436519
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