A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14449606



Internal ID22221698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10129144..10129227hg38UCSC Ensembl
chr21:10607172..10607255hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192354
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)nssv14449606
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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