A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14407660



Internal ID22329085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33320445..33324780hg38UCSC Ensembl
chr21:34692750..34697085hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg384336
hg194336
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197877
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14407660
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