A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459157



Internal ID22252902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40440327..40440550hg38UCSC Ensembl
chr21:41812254..41812477hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201683
Supporting Variants
SamplesHG00733
Known GenesDSCAM
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14459157
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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