A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14407883



Internal ID22293202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8865262..8865320hg38UCSC Ensembl
chr21:9754095..9754153hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209025
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)nssv14407883
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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