A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14432755



Internal ID22175639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8680759..8680854hg38UCSC Ensembl
chr21:9569592..9569687hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205808
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)nssv14432755
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